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Job DescriptionSalary: $22 - $24/hour About BPS Bioscience BPS Bioscience is a leading provider of recombinant proteins, assay kits, and cell lines, specializing in supporting drug discovery across various research areas, including cancer, neurology, immunotherapy, epigenetics, and more. We are dedicated to advancing scientific discovery by offering high-quality products and services to researchers worldwide. Job Overview This role is responsible for the preparation, formulation, and packaging of biochemical reagents and assay components in compliance with ISO 9001:2015 standards. The ideal candidate will thrive in a fast-paced, quality-driven environment and demonstrate strong attention to detail, consistency, and documentation. Success in this role requires a team-oriented mindset, flexibility to adapt to shifting priorities, excellent interpersonal skills, and a commitment to high-quality work. Responsibilities: • Reagent Preparation:Accurately retrieve, weigh, and mix raw materials and components according to department procedures., • Labeling & Packaging:Dispense and label final products with precision, ensuring traceability and compliance with documentation standards., • Documentation:Maintain accurate and complete records of manufacturing activities in both paper and electronic formats, in accordance with ISO 9001 standards., • Inventory Management:Use ERP systems and Labguru ELN software to track material usage, manage inventory, and restock supplies., • Workplace Organization:Maintain a clean and organized work area following 5S principles and safety protocols., • Process Support:Assist in process development and scale-up activities for new reagent formulations, including troubleshooting and optimization., • Cross-functional Collaboration:Work closely with QC, QA, and R&D teams to ensure product quality and support tech transfer initiatives., • Other Duties:Perform additional tasks assigned to support production goals. Requirements: • Bachelors degree in Biology, Chemistry, Biochemistry, or related field required., • 02 years of experience in a manufacturing or laboratory setting, preferably in reagent or assay production., • Familiarity with ISO 9001 or other quality systems is a plus., • Strong organizational and communication skills. Benefits! • 401k with 4% company match, • Medical/Dental/Vision health insurance plans, • Vacation and paid holidays, • Companywide lunches provided quarterly BPS Bioscience Inc. is an equal opportunity employer, without regard to race, color, religion, age, gender, sexual orientation, disability, or any other characteristic protected by applicable law.

Job Description The hours for this position are 10 hour shifts x 4 days per week between Monday - Friday. Exact days to be determined upon hire. JOB SUMMARY The Manufacturing Associate II, Cell Therapy is responsible for performing well regulated GMP aseptic cell culture activities including media preparation, cell thaws, cell expansion, cell harvesting, and cryopreservation using standard cell culture technologies in a cleanroom environment. The Associate will be responsible for following Batch Production Records, Standard Operating Procedures, and work instructions in manufacturing spaces. The Associate will be responsible for participating in the maintenance of critical supplies, equipment, product testing, product storage and product distribution. RESPONSIBILITIES • Experience in aseptic technique, clean room gowning and have knowledge of Good Manufacturing Practices (GMPs)., • Documenting of each task, understanding verifier versus operator functions, following cleaning procedures, and ensuring aseptic processing techniques., • Daily updating of Production spreadsheets, review of completed documents, addressing corrections, and communication of document readiness to management., • Responsible for documenting deviations and reporting deviations to department management, • Receipt and processing of blood, cord, blood, and tissue collection processes under cGMPs., • Execution of colony forming units assay procedures (CFUs), set up samples for sterility testing, performs flowcytometry assays for viability and cell identification., • Responsible for execution of cell culture manufacturing: cell thawing, cell passaging, cell feeding, harvesting, cell counting, cryopreservation, and stability testing., • Performs sample processing, intermediate formulations, storage, and distribution of product, • Operation of supporting equipment for daily manufacturing., • Train on and actively participate in revising of Standard Operating Procedures (SOPs), Batch Production Records (BPRs), Work Instructions, and Forms., • Supports environmental monitoring processes including personnel monitoring, suite monitoring as defined by the facility, • Assist with the weekly maintenance/cleaning of equipment and cleanroom to support GMP production., • Assist Subject Matter Expert (SME) with providing training for new and existing employees., • Assist with the ordering, stocking, release of supplies/materials to meet production demands, • Provides feedback and support in drafting and implementing documents and procedures for department development/process improvement., • Help identify potential equipment or process issues., • Supports the Excellos safety, GMP and Quality Plan., • Participates in department meetings, proficiency testing, and educational programs. WORKING ENVIRONMENT • Normal laboratory environment with biohazard precautions., • Must work with living human cells and various chemicals., • May be exposed to blood or bodily fluids that may be capable of transmitting diseases., • May be exposed to hazardous chemicals., • Will be working with liquid nitrogen., • May be called on to workdays or hours other than routinely scheduled hours, work overtime hours, or potentially work through breaks, if necessary. PHYSICAL REQUIREMENTS • Must be able to stand long hours., • Must be able to sit at biosafety cabinet for hours, while aseptically manipulating product., • Must be able to communicate clearly., • May be required to lift 50 pounds. EQUIPMENT USED • Laboratory processing equipment (examples include, but are not limited to: centrifuges, heat sealers, sterile connecting devices, biosafety cabinets, cell counters, flow cytometers, incubators, bioreactors, cell separators)., • Normal office equipment such as: telephone, computer, cell phone, printer, copier, fax, scanner., • General laboratory equipment (examples include, but are not limited to: barcode scanners, scales, shippers, refrigerators, freezers). QUALIFICATIONS Education: • Bachelor’s degree in cell biology or related field with 1 + years industry experience or • Associate degree in related area and/or a Biotech Program certificate from an accredited college with 2 + years industry experience. Skills: • Strong understanding of aseptic technique and Good Manufacturing Practices (GMP)., • Proficient in standard cell culture methods including cell counts using Hemocytometer, perform calculations including cell concentration determination, seeding densities, % viability, weight measurements, and volume., • Interpersonal skills to establish professional relationships both internally and externally., • Critical thinking, creativity, and innovative thinking., • Detail oriented with the ability to set priorities and organize daily work requirements., • Must be able to work both as a team member and independently, as required., • Proficient in professional communication both written and oral, which is clear and precise., • Must keep Management informed on any technical and/or operational issues that arise., • Must be flexible, as production priorities, timelines, and processes can change regularly., • Integrity and discretion – ability to maintain confidentiality., • Ability to perform under pressure and work under stressful situations. Certifications/Licenses: • Biotech certificate valued, not required

Job Description Job Title: Manufacturing Technician Job Description The Manufacturing Technician will be responsible for performing a range of manufacturing tasks related to reagents and buffers. The role involves troubleshooting formulations, filling processes, packaging, and conducting Quality Control procedures. You will work in a collaborative environment, supporting R&D and process improvement activities to meet production goals. Responsibilities • Perform assigned manufacturing tasks for reagents and buffers as assigned by the Supervisor/Lead., • Troubleshoot formulations, filling processes, packaging, and analytical techniques., • Conduct Quality Control procedures for consumables., • Perform data collection and analysis., • Process work orders to complete products to inventory., • Execute and improve batch records and SOPs., • Identify gaps and weaknesses in SOPs and formulations for finished goods and component materials., • Maintain accurate inventory of materials through cycle counts, ordering, and receipt of materials., • Operate in a fast-paced environment with rapidly shifting priorities., • Work as part of a multi-disciplinary team with other scientists, engineers, and manufacturing personnel., • Lead kit support and line operations., • Perform simple buffer formulation under 50L., • Provide fill support., • Experience with SOPs, BRs, and WIs., • Hands-on experience with pH, conductivity meter, UV-vis, and other standard lab equipment., • Self-motivated with the ability to work independently as well as in teams., • Highly organized and flexible., • Detail-oriented with strong analytical, verbal, and written communication skills., • Experience with developing and updating BOMs is preferred., • Experience with formulation, fill, packaging, and chromatography in a laboratory setting is preferred. The work environment is within a multi-disciplinary startup focused on innovating genetic analysis tools for research and clinical markets. The role requires training in a second shift (2pm - 10:30pm), with potential work in staggered second shift (6pm - 2:30am) and eventually third shift (10pm - 6:30am). Shift differentials apply: 1st shift (6AM-2:30PM) offers regular hourly pay, 2nd shift offers a 5% differential, staggered 2nd shift offers a 7.5% differential. The work environment is dynamic, supporting R&D development and daily needs requests. Job Type & Location This is a Contract to Hire position based out of San Diego, California. Pay and Benefits The pay range for this position is $23.00 - $25.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in San Diego,CA. Application Deadline This position is anticipated to close on Oct 20, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

Job Description FEFA, LLC seeks a Clinical Program Manager to support the Naval Health Research Center (NHRC), Operational Infectious Diseases (OID) Directorate. The OID Directorate conducts ongoing, laboratory-based surveillance of US military populations in unique environments to quantify and study the etiology of infectious illnesses. This position will support research on infectious pathogens affecting military personnel and advance studies related to pathogen biology, host-pathogen interactions, and disease transmission. This role will primarily be responsible for overseeing day-to-day project operations, ensuring contract compliance, managing resources, and serving as the primary point of contact for the client and internal teams. Compensation: $105,000.00-125,000.00 per year. Key Responsibilities: • Lead the planning and implementation of project tasks, ensuring timely execution within scope and budget, • Interface regularly with the client, vendors, and internal stakeholders to ensure effective communication and project alignment, • Develop and maintain project documentation, schedules, and status reports, • Oversee onboarding and tasking of project personnel, ensuring role clarity and resource optimization, • Manage deliverables, track milestones, and proactively identify risks and mitigation strategies, • Provide regular updates to program leadership and ensure client satisfaction Project Management & Coordination • Provides day-to-day supervision of department-based research staff, ensuring efficient coordination of clinical research projects., • Manages the lifecycle of clinical research and bio surveillance studies, from protocol development through study implementation, data collection, and reporting., • Collaborates with internal and external stakeholders, including researchers, clinicians, sponsors, and regulatory bodies, to ensure smooth project execution., • Monitors project timelines, deliverables, and milestones, ensuring adherence to deadlines and budgets. Responsible for writing and reviewing monthly reports Budget Development & Management • Develops, negotiates, and monitors project budgets related to funded research initiatives., • Tracks and manages expenses, ensuring that projects remain within budget and align with the OID Directorate’s financial objectives., • Provides financial reports and updates to leadership, sponsors, and other key stakeholders as required. Regulatory Compliance & Quality Assurance • Ensures that all clinical research projects comply with Institutional Review Board (IRB) requirements, Good Clinical Practice (GCP) guidelines, and relevant federal regulations., • Monitors for quality assurance throughout the clinical research process, conducting regular reviews of data accuracy, regulatory compliance, and adherence to study protocols., • Oversees the preparation and submission of regulatory documents, reports, and study-related correspondence. Staff Supervision & Development • Supervises and mentors clinical research staff, providing guidance and support to ensure high performance and professional growth., • Assigns responsibilities, oversees workload distribution, and conducts regular performance evaluations of clinical research team members., • Facilitates training opportunities for staff to stay current with clinical research best practices, regulatory requirements, and relevant scientific advancements., • Coordinate with public health, clinical, and operational partners to support timely data reporting and analysis. Direct and manage bio surveillance operations, integrating epidemiological data, syndromic surveillance, and lab results to identify and respond to emerging threats. Stakeholder Communication & Reporting • Serves as the primary point of contact for sponsors, funding agencies, and external partners, ensuring timely communication and coordination throughout the project lifecycle., • Prepares and presents project updates, progress reports, and final study findings to NHRC leadership and other stakeholders., • Participates in the writing and editing of scientific publications, abstracts, and presentations related to clinical research findings., • Develop and refine surveillance protocols, data-sharing agreements, and emergency response procedures. Team Leadership & Supervision: • Supervise and mentor a multidisciplinary team of research coordinators, clinical staff, and bio surveillance analysts., • Conduct performance evaluations, facilitate professional development, and support staff in meeting deliverables., • Foster a culture of collaboration, accountability, and scientific integrity. Regulatory & Compliance: • Ensure compliance with IRB requirements, DoD/NIH/FDA policies, and institutional procedures., • Maintain accurate records and support audit readiness through comprehensive documentation., • Manage adverse event reporting, protocol deviations, and other regulatory submissions. Strategic Planning & Communication: • Develop project plans, manage timelines, and lead initiatives under tight deadlines and high-pressure environments., • Support strategic planning for long-term research and surveillance priorities., • Communicate progress and findings clearly to leadership, sponsors, collaborators, and external partners. Other Duties as Assigned Qualifications: • Bachelor’s degree in Science, or related field (Master’s in public health or business is preferred), • PMP or equivalent project management certification (preferred), • Minimum 5 years of experience managing research projects/programs or similar complex projects with at least 2 years in a supervisory or leadership role, • Strong working knowledge of project management software (e.g., MS Project, Smartsheet), • Excellent communication, leadership, and organizational skills · Familiarity with REDCap, CTMS, or other clinical trial management platforms. · Clinical research certification (e.g., CCRC, CCRP) strongly preferred. Soft Skills Required: · Proactive Leadership & Communication: Effectively leads cross-functional teams, fosters collaboration, and communicates complex concepts clearly across clinical, research, and operational stakeholders. · Adaptability Under Pressure: Maintains composure and focus in high-stakes environments, adjusting to evolving priorities and tight timelines without compromising quality. · Strategic Thinking & Problem Solving: Anticipates challenges and identifies solutions, continuously looking for research growth opportunities, in both clinical trials and bio surveillance settings. · Emotional Intelligence & Team Development: Builds trust, supports staff development, manages change and demonstrates empathy and professionalism in all interactions. Some positions or sites may require that the incumbent be fully vaccinated against COVID-19, and proof of vaccination may be required. Benefits FEFA, LLC is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. We offer a competitive compensation package including a competitive salary, medical benefits, PTO, holiday pay and more.

Job Description What We Do: Calidi Biotherapeutics is a clinical-stage immuno-oncology company with proprietary technology that is revolutionizing the utilization of oncolytic viruses through an allogeneic cell-based delivery system. Calidi Biotherapeutics is advancing this potent stem cell and oncolytic virus combination for use in multiple difficult-to-treat oncology indications. Our team is also developing a universal cell delivery system to protect, amplify, and potentiate oncolytic viruses currently in development. Job Overview/Summary: The Senior Associate I, Quality Control contributes to the quality of Calidi’s products and processes by overseeing external laboratory testing of GMP materials. This includes assurance that laboratory results are timely, reliable, and in accordance with all applicable regulatory requirements and internal procedures. This role collaborates cross functionally to develop, transfer, and qualify analytical methods, maintain global GMP inventory, qualify new suppliers, and support the strategic leadership of daily QC operations. Additionally, this position has supply chain tasks for inventory, clinical trial distribution, and sample logistics in compliance with regulatory standards. Ensures timely and efficient delivery of pharmaceutical products and materials across global operations while maintaining quality and traceability. Responsibilities: • Oversees external laboratory testing of GMP starting materials, in-process, release, and stability samples to ensure testing is performed in accordance with applicable internal procedures and specifications., • Reviews and approves QC procedures, test results, reports and production batch records. Conducts investigations into any out-of-specification results or laboratory deviations., • Implements appropriate corrective and preventive actions to address root causes and prevent recurrence., • Coordinates contract laboratory vendors, monitors laboratory performance, assesses capability, and ensures actions are taken to improve, as needed., • Troubleshoots challenges while fostering a collaborative approach with external partners to support seamless and reliable QC operations., • Coordinates the stability testing programs for GMP materials, including reviewing stability data and reports, comparing test results against stability specifications, and establishing retest dates as appropriate., • Builds and maintains expertise in QC analytical processes and methods critical to oncolytic virus and cell therapy product development, manufacture, characterization, and release., • Supports development of test methods and procedures., • Facilitates method transfer from internal development to external partners, including overseeing laboratory testing during method qualification and validations activities., • Collaborates with Manufacturing to ensure incoming raw materials and components meet necessary quality requirements., • Works with Quality Assurance and external vendors to qualify new suppliers, implement appropriate sampling and testing of incoming materials, and review supplier-provided quality documentation., • Inventories GMP products and materials, including reference standards and critical reagents used in routine testing., • Prepares and maintains appropriate permits and documentation to support global shipment of regulated materials., • Provides CMC support on product development efforts related to formulation development, drug delivery device, container closure selection, packaging and labeling., • Collaborates with internal and external Manufacturing, Quality Assurance, Regulatory Affairs, and Development teams to support overall CMC activities of projects in the pipeline., • Participates in cross-functional meetings to address project timelines, tech transfer, and align on project objectives., • Plans and implements continuous improvement of methods, processes, and systems to assure compliant manufacturing of products., • Addresses inventory levels across multiple sites, ensuring accuracy, availability, and compliance with GMP/GDP standards., • Guides domestic and international shipping of products and ensure chain of custody, proper handling, storage, and transportation of temperature-sensitive and controlled substances., • Coordinates clinical trial material distribution, including investigational medicinal products and material supply as needed., • Leads sample logistics processes, including biological sample tracking, shipment coordination, and chain-of-custody documentation., • Develops and support all SOPs and procedures required to perform tasks related to supply chain, • Inform Technical Operations leaders as to progress, barriers/issues needing resolution and maintenance of timelines., • Other duties as assigned. Qualifications: • BS or higher degree in Life Sciences, Chemistry, or a related field (e.g., Chemistry, Biology, Immunology, Microbiology) and formal training in cGMP, cGCP, cGLP, regulatory requirements, • Minimum of 5 years of experience in a QC role in a GMP manufacturing environment., • Proven track of supply chain activities., • Broad knowledge of QC processes and procedures, LIMS systems, and GMP regulations and guidance with demonstrated effectiveness in maintaining QC processes for compliance with regulations., • Excellent organization and project management skills. Mathematical Skills: • Ability to work with mathematical concepts such as calculation of dilutions and statistical analyses., • Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations. Reasoning Ability: • Ability to define problems, collect data, establish facts, and draw valid conclusions. Language Skills: • Ability to read and understand technical procedures., • Ability to write protocols and reports., • Ability to effectively present data and respond to questions from co-workers., • Good verbal and written communication skills. The Perks: • Breakroom snacks and beverages, • Competitive Total Rewards package (Medical, Dental, Vision) offered to full-time employees, • Stock options Work Location: Calidi Biotherapeutics employment provides the opportunity to work in beautiful San Diego, California only minutes from the nearest beach. EOE and Accommodation We value diversity and are proud to be an Equal Opportunity and Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law. Calidi Biotherapeutics provides reasonable accommodation in job application procedures for qualified individuals with disabilities and disabled veterans. If you need accommodation in connection with the recruiting process due to a disability, you may let the recruiting contact know. If you are selected to interview for a position, you may also request an accommodation with our team directly. Notice to Agency and Search Firm Representatives: Calidi Biotherapeutics is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Calidi Biotherapeutics employee by a third-party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Calidi Biotherapeutics. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Employer’s Rights: This job description does not list all the duties of the job. You may be asked by supervisors or managers to perform other duties. You will be evaluated in part based upon your performance of the tasks listed in this job description. The employer has the right to revise this job description at any time. The job description is not a contract for employment, and either you or the employer may terminate employment at any time, for any reason.

Expertise in molecular biology techniques such as PCR, Western blotting, flow cytometry, and immunocytochemistry.

Proficiency in molecular biology techniques such as PCR, Western blotting, and immunocytochemistry.

Job Description We are seeking a Senior Provider Partnerships Representative to lead the development of high-impact referral relationships and strategic joint ventures with healthcare providers throughout the San Diego and Orange County region. This role will be critical in accelerating patient acquisition, improving care coordination, and building long-term value with referring partners across the healthcare continuum. The ideal candidate brings deep knowledge of the local healthcare ecosystem, strong relationship-building skills, and a track record of driving referral growth through provider engagement. Key Responsibilities * Build & Manage Referral Partnerships * Identify and nurture high-potential referral sources, including health systems, primary care providers (PCPs), psychiatrists, therapists, emergency departments, inpatient psychiatric units, partial hospitalization programs (PHPs), and outpatient behavioral health clinics. Design and implement targeted outreach strategies to expand Salma’s referral network in alignment with our patient population and clinical capabilities. * Represent Salma in the field by coordinating and attending in-person meetings, events, and educational sessions to strengthen relationships with referring partners and increase brand visibility. * Facilitate the development and execution of Memoranda of Understanding (MOUs) to formalize referral partnerships, clarify shared goals, and ensure alignment around care coordination and communication expectations. * Support Local Market Development * Collaborate with marketing and operations to localize messaging, co-host provider events, and track referral funnel performance * Analyze referral data and optimize for high-performing channels and relationships * Maintain CRM & Performance Metrics * Track activity, outreach, and conversion metrics in CRM * Build and maintain dashboards on referral volume, partner engagement, and provider satisfactio Qualifications * 3-5 years of experience in healthcare business development, provider relations, partnerships, or strategic sales * Deep familiarity with the San Diego or Orange County provider landscape; existing relationships a plus * Strong understanding of behavioral health, primary care, or specialty care (e.g., physical therapy, mental health, pain management) * Experience driving referral growth in a clinical setting or developing partnerships with physician groups, hospitals, or health systems * Excellent communication, negotiation, and relationship management skills * Self-starter who thrives in a fast-paced, field-oriented role Company Mission & Vision: We are the brain health company of the future that integrates care delivery, technology innovation and research breakthroughs to better understand brain biology and diagnose, treat and ultimately cure brain disorders for all stages of life. Compensation & Benefits: * Base (Salary or Hourly Rate): $80,000-100,000 depending on experience, qualifications, and location * Incentives: Incentive bonus structure as well * Benefits: Medical, dental, vision, PTO, and additional benefits We reserve the right to modify benefit offerings at any time, in accordance with applicable laws. Company DescriptionAbout Kaizen Brain Center Kaizen Brain Center is a concierge neurocognitive clinic located in La Jolla & Orange County, CA. We provide state-of-the-art, evidence-based care for individuals with psychiatric and neurological conditions, including Treatment-Resistant Depression (TRD), PTSD, Memory Disorders, Traumatic Brain Injury (TBI), and migraine-related cognitive and mood dysfunctions. We combine cutting-edge science with a personalized care model to offer comprehensive evaluation and treatment in one convenient location.About Kaizen Brain Center\r\nKaizen Brain Center is a concierge neurocognitive clinic located in La Jolla & Orange County, CA. We provide state-of-the-art, evidence-based care for individuals with psychiatric and neurological conditions, including Treatment-Resistant Depression (TRD), PTSD, Memory Disorders, Traumatic Brain Injury (TBI), and migraine-related cognitive and mood dysfunctions.\r\nWe combine cutting-edge science with a personalized care model to offer comprehensive evaluation and treatment in one convenient location.

Job DescriptionSenior Scientist, Potency Assay Location: San Diego, CA Employment Type: Full-time Hiring Company: BioPhase (on behalf of our client) Pay: $145,000–$165,000 base + bonus; stock options Hours: Monday–Friday, full-time Job Description: We’re seeking a Senior Scientist to develop and qualify target-binding and cell-based potency assays for protein biologics and conjugates. You’ll own assay strategy from discovery through CMC, and lead method transfer/implementation at CDMOs for lot release, stability, and characterization in support of clinical manufacturing. Essential Duties and Responsibilities: • Build GMP QC-compatible target engagement and cell-based potency assays for multiple modalities., • Culture/maintain cell lines and create well-documented cell banks for assay use., • Identify, qualify, and manage critical reagents; maintain assay readiness., • Author/review development reports, method transfer/verification/qualification protocols, and summaries., • Review GMP release/stability results; support OOS/OOT investigations, QC data review, and batch release at partner sites., • Partner with CDMOs on reference standard qualification and assay lifecycle management., • MS/PhD in Biology, Biochemistry, or related field., • 5+ years’ industry experience developing potency assays., • Hands-on expertise qualifying recombinant and cell-based assays (target binding, signaling, cytotoxicity) for GMP use., • Proficient with data analysis tools (e.g., GraphPad Prism, SoftMax Pro)., • Prior CDMO collaboration and exposure to regulatory filings.

Job DescriptionCompany Description Eurofins Scientific is a network of independent companies providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. With more than 20 U.S. locations, Eurofins Built Environment Testing offers Industrial Hygiene (IH) and Indoor Air Quality (IAQ) services to protect health in built environments. Clients include consultants, industry, real estate, healthcare, government, and homeowners. Services cover a wide range of tests, including asbestos (PLM/TEM), mold, bacteria, VOCs, allergens, Legionella, radon, lead, silica, and more. Job Description The Lab Manager will manage a team of Mold and Asbestos Analysts and other Laboratory staff, provide leadership and be responsible for ensuring compliance of laboratory operations. Will help maintain/adjust workflow to meet TAT, make recommendations, as needed, to improve laboratory functionality, and supervising staff. Will be responsible for ensuring compliance and integration of facility operation with quality assurance, ethics, safety and other corporate and regulatory policies and procedures. Essential Duties and Responsibilities 1. Provide leadership and manage/assist other staff members in the operational team., 2. Assists with the coordination and timely completion of all analytical and operational training for the local lab staff., 3. Prepare and analyze aerobiological, environmental, and water samples for fungal, asbestos and bacteria analysis., 4. Serve as an operational point of contact for clients regarding all services performed in the lab., 5. Coordinates with the local salesperson to assist with client concerns., 6. Determines the local client needs and leads the effort in adding new testing services as needed to meet the local client needs., 7. Coordinates the work of the local lab and assists in setting work priorities to minimize costs, scheduling conflicts or delays., 8. Reviews and modifies group schedules based on current and projected workloads and staffing. Prioritizes the activities of the groups to ensure key goals are achieved and customer service needs are addressed. Manage personnel schedules for Monday-Friday and Tuesday-Saturday staff., 9. Builds and maintains positive customer relationships through direct interaction with customers, project managers, and sales personnel., 10. Fosters morale and teamwork. Fulfills supervisory responsibilities with direct reports to achieve strong staff performance. Mentors key employees., 11. Demonstrates and promotes the company vision. Communicates facility-specific goals and objectives to employees. Communicates and implements company initiatives designed to foster teamwork and communication., 12. Establishes and maintains an active and positive safety culture and ensures that the Employee Health and Safety procedures are implemented and followed to maintain facility operations that are compliant with appropriate policies and regulations., 13. Reviews SOPs used in the facility and ensures their implementation so that the facility is operated in a compliant manner which allows it to produce defensible data., 14. Supports the Human Resources function to ensure that all policies and programs are applied consistently throughout the laboratory. Secondary Duties 1. Remains current on new technological developments and provides scientific leadership in establishing new analytical services as needed, works with Technical Director., 2. Assists the QA manager in development, implementation, and data collection of QA processes for the different analytical tests., 3. Assists in pursuing, receiving, and maintaining necessary laboratory accreditations., 4. Recommends and coordinates sample transfer as necessary., 5. Assists co-workers with analytical questions as necessary., 6. Ordering and inventory control for lab supplies and equipment. • Strong Professional background in working with Mold and Asbestos Samples, • Previous Supervisory/Management experience required, preferably 2 yrs., • BS degree in Microbiology, Biology, or equivalent degree, • Minimum 3 years of previous hands on laboratory experience Additional Information Compensation Range: candidates who qualify with minimum requirements start at $75,000 annually. Higher compensation will be considered for more qualified experienced candidates. Position is full-time, exempt status. Experienced and qualified candidates are encouraged to apply. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options. We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2024, Eurofins generated total revenues of EUR 6.95 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description Who we are: Biosero, Inc. is the leader in life science robotic automation and integration. Our award-winning no-code software tools enable vital research to be done quickly while freeing scientists to address additional scientific challenges. Our solutions are placed in the top accounts worldwide, including the top: pharmaceutical, agricultural, clinical, diagnostics, and biotech companies. Our work impacts the world by accelerating productivity, discovery & cures. Our team is passionate about our mission to enable discoveries in life science by coupling our software platforms with data and robotics. Biosero is the fastest-growing software company in the life sciences space. We have been voted the best place to work for many years. Biosero is part of the BICO Group. BICO is the leading bio convergence company in the world, equipping hundreds of laboratories and thousands of scientists with cutting-edge life science technologies. By combining different technologies, such as robotics, artificial intelligence, computer science, and 3D bioprinting with biology, BICO enables customers to improve people's health and lives for the better. Biosero is seeking an accomplished and visionary Head of Strategy & Product Management to define and drive the company’s long-term strategic direction while translating it into actionable product roadmaps. This executive will lead the product management function, shape the overall portfolio, and ensure alignment with market needs and customer value. As a key member of the Biosero leadership team, the Head of Strategy & Product Management will also serve as an external ambassador, representing the company at industry events, customer forums, and partner engagements. Responsibilities: Strategic Leadership • Define and continuously refine Biosero’s overall business and product strategy in alignment with corporate objectives., • Partner with the Managing Director and leadership team to identify and execute growth opportunities, both organic and inorganic., • Own the end-to-end product management function, including vision, roadmap, and lifecycle management., • Translate strategic goals into prioritized development initiatives, balancing innovation, customer requirements, and commercial impact., • Collaborate closely with R&D, software engineering, and operations to ensure timely delivery of roadmap milestones., • Partner with commercial teams to gather customer insights and translate feedback into product enhancements., • Aligning with finance and operations to ensure product decisions are financially sound and operationally scalable., • Represent Biosero at key industry events, scientific conferences, and customer advisory boards., • Act as a thought leader in automation software and digital transformation within life sciences., • 12+ years of experience in strategy, product management, or general management, ideally within life sciences, automation, or laboratory software industries., • Proven success in developing corporate strategies and building product roadmaps that drive growth., • Demonstrated leadership experience in building and managing high-performing product teams., • Strong analytical, problem-solving, and communication skills., • Ability to balance visionary thinking with disciplined execution., • Strategic thinker with strong business acumen., • Customer-centric mindset with a deep appreciation for the scientific community., • Collaborative leader who thrives in cross-functional environments., • Confident communicator and public speaker. All employment decisions at Biosero & BICO US are based on individual merit, qualifications, and business needs. We are dedicated to providing an inclusive and equitable workplace where all employees and applicants have the opportunity to succeed. Biosero provides equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, sexual orientation, national origin, age, disability, veteran status, gender identity, or any other factor protected by applicable federal, state, or local laws. In addition, Biosero complies with applicable state and local laws governing nondiscrimination in employment in every location in which it has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. Biosero is committed to diversity and inclusion. We seek individuals from all backgrounds and appreciate and celebrate the diversity of our growing team. Powered by JazzHR Xcq85NJP5s

Job DescriptionSalary: $90,000 - $100,000/year Job Overview BPS Bioscience Inc. is a leading provider of recombinant proteins, assay kits, and recombinant cell lines for drug discovery. We are seeking an exceptional scientist, with a strong background in enzymology, enzyme kinetics, protein/protein interactions, and fluorescence and luminescence-based assays. The Scientific Communications Manager will support BPS Bioscience through product marketing efforts and scientific content. More specifically, this rolewill provide in-depth scientific and technical support in relation to solutions for the marketplace and product marketing. Responsibilities: • Creates and develops product/portfolio marketing strategies., • Participates in or leads problem solving and troubleshooting activities., • Writes and coordinates the development of scientific content for: product pages, webinars, technical notes, posters, blog posts, marketing collateral., • Ensures customer needs are identified and addressed via creation and updates to product literature and service guides., • Finalizes new product launches daily with technical review and editing of product inserts and web content., • Partners closely with product management and scientific teams to gain an understanding of product features and relevance to market segments., • Participates in writing of Standard Operating Procedures (SOPs) for the Marketing team., • Creates sales enablement tools including webinars, support content and other relevant content., • Monitors and reports scientific/technical knowledge of scientific fields and their potential impact to products in the market., • Keeps up to date with new trends in drug discovery., • Attends scientific meetings to support business objectives., • Other duties as assigned. Requirements: • Ph.D. in Immunology, Cancer Biology, or Molecular Biology & Cell Biology, • A minimum of 2+ years of experience in the Life Science industry, • Must be able to build credibility and relationships across functions and levels, • Ability to communicate with and influence internal and external audiences, using both oral and written communication skills highly effectively, • Excellent writing skills, • High level of organization, multi-tasking, and attention to detail Benefits! • 401k with 4% company match, • Medical/Dental/Vision health insurance plans, • Vacation and paid holidays, • Companywide lunches provided quarterly BPS Bioscience is an equal opportunity employer, without regard to race, color, religion, age, gender, sexual orientation, disability, or any other characteristic protected by applicable law.

Job Description Overview Ansible Government Solutions, LLC (Ansible) is currently recruiting Medical Technologists to support the VA Medical Center located at 3350 La Jolla Village Dr, San Diego, CA 92161. Services will be delivered to both the Anatomic Pathology and Clinical Pathology divisions of the facility. Exceptional compensation packages with full benefits are available. Ansible Government Solutions, LLC (Ansible) is a Service-Disabled Veteran-Owned Small Business (SDVOSB) providing Federal customers with solutions in many arenas. Our customers face wide-ranging challenges in the fields of national security, health care, and information technology. To address these challenges, we employ intelligent and committed staff who take care of our customers’ success as if it is their own. Responsibilities • Rotate on a regular basis through the areas in which they have been trained and are competent, • Perform a broad range of laboratory procedures in Chemistry, Hematology, Coagulation, Urinalysis, Microbiology, and Transfusion Medicine, • Perform advanced and complex laboratory procedures, recognizing deviation from expected results, analyzing and correcting problems using scientific principles, • Recognize and communicate pre-defined critical results affecting patient care, • Maintain the optimal functioning of laboratory equipment and keep appropriate records for documentation; operate, calibrate, identify malfunctions, repair and perform preventive maintenance of laboratory analyzers, • Perform and document quality control, quality assurance and corrective actions related to test performance using sound statistical principles and theories of performance improvement, • Enter and verify laboratory results in the computer system; recognize deviations from expected results, analyze and correct problems using scientific principles, • Accredited Bachelors degree including 16 semester hours in biological science (one course in microbiology), 16 semester hours in chemistry (one course in organic or biochemistry), and one course in mathematics AND two (2) years of post-certification clinical laboratory experience within the last ten (10) years as a certified Medical Laboratory Technician (ASCP-BOC), • A minimum of one (1) year of Medical Technologist experience within the last three (3) years, • Demonstrated knowledge of laboratory medicine techniques and practices, • Demonstrated education and clinical training in the practice of laboratory medicine All candidates must be able to: • Sit, stand, walk, lift, squat, bend, twist, and reach above shoulders during the work shift, • Lift up to 50 lbs from floor to waist, • Lift up to 20 lbs, • Carry up to 40 lbs a reasonable distance Powered by JazzHR 9oKusGlLSA

Job Description Job Summary The Director, Non-Clinical Development will lead a team of toxicologists supporting programs across research and development, providing scientific and strategic leadership for non-clinical safety evaluation from discovery through late-stage development. This role will define and implement non-clinical development strategies, oversee toxicology studies, and ensure high-quality data generation to support regulatory submissions and clinical advancement. The position requires strong collaboration in a matrixed environment and direct engagement with senior leadership, regulatory authorities, and cross-functional partners. Key Responsibilities * Serve as the toxicology lead on multidisciplinary teams, developing and executing non-clinical safety strategies for new therapeutic candidates. * Evaluate potential safety and toxicity risks across programs from early discovery through regulatory filing. * Design and oversee non-clinical safety studies to assess relevance and translatability of findings to humans. * Manage internal and external study execution, including CRO oversight, protocol development, monitoring, and data interpretation. * Collaborate closely with cross-functional teams such as Biology, Biomarkers, and PK/PD to integrate non-clinical and translational insights into development plans. * Draft and review non-clinical sections of regulatory submissions, including INDs, IMPDs, CTAs, and Investigators Brochures. * Participate in regulatory interactions with agencies such as the FDA, EMA, and PMDA to discuss non-clinical strategy and data packages. * Manage external vendor relationships, budgets, and timelines, ensuring compliance with applicable regulations. * Lead, mentor, and develop a team of toxicologists, fostering scientific rigor, collaboration, and professional growth. * Contribute to publications, presentations, and scientific engagement with external stakeholders and the broader research community. Qualifications * PhD or MS in Toxicology, Pharmacology, Pathology, or a related field; post-doctoral experience preferred. * 10+ years of experience in non-clinical or regulatory toxicology (15+ years for MS-level candidates). * Experience with biologics and/or oligonucleotide-based therapeutics preferred. * Strong understanding of GLP regulations and global regulatory guidelines (FDA, EMA, ICH). * Demonstrated success managing CRO relationships, toxicology studies, and regulatory submissions. * Proven ability to influence cross-functional teams and operate effectively in a matrixed organization. * Excellent communication, presentation, and leadership skills with a collaborative, solution-oriented mindset. * Ability to work independently, prioritize multiple projects, and thrive in a fast-paced research environment.

Job Description Research Scientist, Antibody Discovery and Research Job #25-07A Mapp Biopharmaceutical, Inc. "Mapp" is a San Diego based, innovative biopharmaceutical company focused on addressing unmet medical needs through the development of life-saving monoclonal antibody treatment options to combat a variety of neglected and tropical infectious diseases, and in support of biodefense programs. The Early Research and Development Group (ERDG) and the Advanced Research and Development Group (ARDG) at Mapp Biopharmaceutical are responsible for the execution of high quality Research and Development activities to ensure the achievement of a robust portfolio through CMC, Nonclinical, Regulatory, Project Management, and Clinical activities consistent with Mapp's product development objectives. The Research Scientist works in the antibody discovery group which is responsible for isolating novel antibodies that may be used in future drug products. This includes creating and producing the antigens necessary to isolate these antibodies and assessing the antibodies for their potential as therapeutics. The Research Scientist, Antibody Discovery and Research will provide overall support for our projects including design, execution, supervision, analysis and interpretation of results. Basic Qualifications • PhD or equivalent in biology, molecular biology, biochemistry, virology, and/or related field, • Post doc experience or other appropriate scientific experience, • Author on scientific publications in respected peer reviewed journals, • Demonstrated excellence in the following competency areas:, • Protein expression in bacterial, mammalian and insect cell systems, • Protein purification, including experience with automated HPLC and FPLC systems, fluency in GE Unicorn FPLC software, • Flow cytometry and single B-cell sorting techniques, • Experience in leading scientific personnel to execute against program deliverables, • Experience with ForteBio Octet technology and isothermal titration calorimetry, • Hands-on experience operating IncuCyte and similar high-content live-cell imaging systems, • Experience with primer design and RT-PCR particularly for monoclonal antibody isolation and cloning from single B-cells, • Experience expressing and purifying viral proteins, • Experience with reverse genetics and pseudo typed viral vector systems., • Command of in-silico workflows for antibody and protein engineering and optimization, • Development of functional cell based assays/immunoassays to assess mechanism of action and potency of new antibody candidates (e.g. reporter assay, internalization assay, neutralization assay, shedding assay ADCC-assay, ADCP-assay, multi-color flow etc.), • Optimizes and designs expression constructs for protein stability, solubility and expression levels, • Designs and optimizes strategies to generate and purify proteins of interest for subsequent in vitro and in vivo applications, • Designs and develops novel in vitro assays to assess antibodies for binding and activity, • Supervises research scientists at various levels as needed, • Reviews and synthesize new research findings regularly, • Maintains detailed records of all experiments performed This position is an on-site position located in Mapp's new state-of-the-art San Diego facility. Willingness to Travel (Domestic Travel = Approximately 2x per year + International Travel = Approximately 1x per year) will be required for this position. Mapp wants you to join their team and invites you to apply by submitting your information through the Mapp Biopharmaceutical, Inc. Job Openings website page. This job will remain open for twenty (20) days after being posted on Mapp's Job Openings website page. No Solicitors, agents or placement agencies please. Mapp utilizes E-Verify. Mapp is an equal opportunity employer and employment decisions are not based on any protected status. Mapp uses a wide variety of advertising and outreach to find qualified applicants for employment. Mapp is an Equal Opportunity Employer/Veterans/Disabled. Job Posted by ApplicantPro

Job Description Sanford Burnham Prebys is much more than a research facility and hub for innovation; it’s a vibrant global community of talented scientists and researchers from over 30 countries. This worldwide representation enriches our perspectives and enhances our creative approach to solving complex scientific challenges. We strive to be leaders not only in biomedical research but also in creating an environment where excellence thrives through collaboration across cultures and backgrounds. Our mission is to advance the biomedical sciences by cultivating the next generation of scientific leaders, providing meaningful opportunities for researchers of all backgrounds to learn, innovate, and make breakthrough discoveries that improve human health. Together, we translate science into health. The duties and responsibilities contained in the job description are intended to be examples of the accountabilities for which the person in the position will demonstrate competency through performance. The job description is not intended to be an all-inclusive list. Duties and responsibilities are subject to change and other duties may be assigned as necessary. Summary: The Commisso Lab at Sanford Burnham Prebys is seeking a highly motivated Research Associate to join our dynamic team focused on cutting-edge drug discovery in pancreatic cancer. Our laboratory is at the forefront of exploring innovative strategies to target tumor metabolism and uncover new therapeutic vulnerabilities. Supported by a multidisciplinary collaboration with drug discovery experts, this position offers a unique opportunity to be directly involved in translational science with the potential to impact patient care. The Research Associate will play a central role in designing, executing, and analyzing experiments that drive our discovery pipeline—from high-content and high-throughput fluorescent assays to cell-based studies of proliferation, survival, and protein function. Beyond hands-on bench science, the successful candidate will coordinate with internal and external collaborators, manage project logistics, and contribute to the preparation of data for presentations, manuscripts, and grant applications. This is an exciting opportunity to work at the interface of cancer biology and therapeutic innovation in a highly collaborative and supportive research environment. Duties and Responsibilities: • Plan, perform, and troubleshoot cell-based in vitro experiments, including high-throughput and medium-throughput fluorescent assays, cell proliferation, cell death, and protein-based assays, • Work within a team-based setting to analyze the experimental results and generate figures and presentations for internal team meetings, • Maintain accurate and detailed laboratory records. Minimum Qualifications: • Bachelor of Science degree in a biomedical field such as Biochemistry, Cell Biology, Physiology, Molecular Biology, Pharmacology, or a closely related discipline., • At least 3 years of full-time laboratory experience in an academic or industry research setting., • Demonstrated hands-on expertise performing cell biology assays, including routine handling and maintenance of human cancer cell lines., • Prior experience performing medium-throughput or high-throughput assays with human cells and familiarity with automated imaging systems, • Background in a drug discovery or translational research environment., • Familiarity with advanced assay platforms for evaluating cell proliferation, cell death, or protein-based readouts., • Must be flexible to work various schedules and hours, including weekends and holidays when necessary., • Strong work ethic, self-motivation, and ability to adapt in a fast-paced, dynamic team environment., • Excellent time management, organizational, and communication skills with a high level of attention to detail., • Professional proficiency with Microsoft Office applications (Word, Excel, PowerPoint), GraphPad Prism, ImageJ/Fiji, and other common research software., • Ability to prepare clear and accurate data presentations, figures, and reports for internal audiences., • Strong analytical and problem-solving skills, with the ability to troubleshoot technical challenges independently., • Commitment to maintaining rigorous scientific standards, reproducibility, and adherence to laboratory safety protocols., • Ability to collaborate effectively with colleagues at all levels, while also working independently when required. None. Compensation: The expected hiring range for this position is $43,703.00 - $54,629.00 commensurate with experience. We welcome talented individuals of all backgrounds regardless of gender, sex, religion, race, national origin, citizenship, age, disability, perceived disability, pregnancy, pregnancy-related condition, reproductive health decisions, sexual orientation, gender identity, gender expression, genetic information, HIV/AIDS, marital status, covered veteran status, or any other characteristic protected by local, state, or federal laws, rules, or regulations. We are proud to be an equal employment opportunity employer. As part of this commitment, Sanford Burnham Prebys Medical Discovery Institute will ensure that persons with disabilities are provided reasonable accommodations for the hiring process. If a reasonable accommodation is needed, please contact our Benefits Team at (858) 646-3100 or via e-mail at

Job Description Job Description: We are seeking a highly motivated and qualified individual to join our Discovery Biology Department as a Senior Director-Executive Director and work as part of a team to drive success. Ideal candidates will be self-motivated, independent, committed to the generation of high-quality data within a fast-paced and innovative research team. This role is ideal for a scientific leader with deep expertise in molecular biology, RNA therapeutics, or gene modulation technologies, who thrives in a fast-paced, collaborative environment. The successful candidate will help shape and drive strategic discovery programs from early target validation through to clinical candidate nomination. Essential Responsibilities: • Scientific Leadership & Strategy, • Provide strategic and scientific leadership across RNA-editing drug discovery programs., • Define biology strategy aligned with corporate goals and pipeline priorities., • Contribute to the preparation of research reports and presentations for internal project teams, leadership team, and external audience., • Program Oversight, • Lead cross-functional discovery teams from early validation through IND-enabling stages., • Design and oversee execution of cell-based, biochemical, and in vivo assays to support SAR and mechanistic understanding., • Innovation & Technology Development, • Carry out assigned laboratory functions applying knowledge and skill in an accurate, timely manner., • Partner with Functional Genomics to identify and evaluate novel targets amenable to RNA editing., • Champion adoption of innovative platforms and models to improve translation and reduce timelines., • Team Building & Mentorship, • Develop and promote a work place culture that values diversity of thought, promote integrity and create an atmosphere that supports coaching and fosters accountability., • Hire, mentor, and manage a high-performing team of scientists and research associates., • Collaboration & Communication, • Serve as key biology lead on multidisciplinary program teams including chemistry, pharmacology, and translational science members., • Establish and maintain excellent working relationships with critical collaborative partners throughout the company., • Present program updates to executive leadership, partners, and at scientific conferences., • Manage external collaborations and CROs to drive timelines and deliverables., • Maintain updated and well-organized lab notebooks., • Execute daily laboratory operations with an approach designed to minimize risks and hazard waste streams., • Maintain all appropriate corporate standards for facility safety and hazardous material management. Reasonable accommodation(s) may be made to enable qualified individuals with disabilities to perform the essential functions of a job, on a case-by-case basis. On-Site Protocol: Physical presence at the ADARx Pharmaceuticals worksite is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture. Qualifications: • Ph.D. in Cell Biology, Molecular Biology, Pharmacology, or related field., • 10–15+ years of industry experience, including 5+ years in a leadership role., • Demonstrated success advancing discovery programs from concept to candidate nomination., • Understanding of project timelines and deliverables and plans/coordinate project work accordingly with departmental, functional, and external stakeholders., • Proven ability to lead and inspire project teams; experience managing scientists and working with CROs/academic collaborators., • Strong problem-solving skills and a proactive attitude towards exploring new approaches., • Excellent written and verbal communication skills and effective presentation of complex scientific data to cross-functional and senior management teams are essential for this role., • Broad knowledge of scientific experience with track record of scientific achievement demonstrated by peer-reviewed publications., • Experience executing verification studies is required., • Deep expertise in molecular and cellular assay development; experience with RNA-editing or gene therapy modalities is a strong plus., • Must be able to work independently as well in cross-functional team settings with supervision as needed., • Adaptable / Flexible - willing and able to adjust to multiple demands and shifting priorities as well as an ability to meet day-to-day challenges with confidence and professionalism., • This is a full-time position, Monday-Friday, occasional overtime., • Pay is commensurate with experience., • Equity-based compensation, • Performance-based bonuses, • 401(k) with Company Match, • Medical, Dental, Vision, • Flexible Spending Account, • Life Insurance, • Employee Assistance Program, • Employee Discounts, • Gym Membership, • Paid Vacation, • Paid Holidays, • United States (Required), • Background Check Company Overview: We are a late-stage clinical biotechnology company dedicated to transforming cutting-edge science into next-generation RNA medicines across a wide range of therapeutic areas. Our goal is to control the expression of specific disease drivers with highly selective RNA targeted therapies, delivering life-changing treatments for patients with urgent unmet medical needs. Disclosure Statement: • The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position., • Data: Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations., • Recruiters & Staff Agencies: ADARx Pharmaceuticals (ADARx) does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to ADARx or its employees is strictly prohibited unless contacted directly by the Company’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of ADARx and the Company will not owe any referral or other fees with respect thereto., • Compensation: The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual target bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, type and length of experience within the industry, and other job-related factors permitted by law., • Total Compensation: Includes base salary; benefits: medical, vision, and dental insurance; life insurance; 401(k) matching program; paid time off; paid holidays; Employee Assistance Program; and other employee benefits. This role may also be eligible for short-term or long-term incentive compensation, including but not limited to cash bonuses., • Conditional Offer of Employment: Following a conditional offer of employment, satisfactory completion of a background check (including criminal records check) is required prior to beginning employment. Any offer of employment may be rescinded if the background check reveals disqualifying information, and/or it is discovered that the candidate knowingly withheld or falsified information. Failure to satisfactorily complete the background check may affect the continued employment of a current NAI employee who was conditionally offered the position.

Job Description We have an immediate need for a Paleontologist. This is an On-call position working on projects throughout California. This individual will be responsible for conducting paleontological monitoring of construction projects to include data collecting, interpretation of stratigraphic units, and salvaging of fossils. Qualifications • BS or BA degree in Geology or Paleontology and one year experience monitoring in the state or geologic province of the specific project AS or AA in Geology, Paleontology, or Biology and demonstrated two years’ experience collecting and salvaging fossil materials in the state or geologic province of the specific project., • Ability to identify vertebrate, invertebrate, plant, and trace fossils to class or lower taxonomic level in the field is desirable, • Ability to travel Upon a conditional job offer, a drug test and background check will be required. Compensation based on experience. (Paleontologist, Geology, Monitoring, Fossils, Geologic Province, Plants, Biology) Company DescriptionAbout us: 347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website us:\r\n\r\n347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website .

Job Description R&D Partners is seeking to hire a SCIENTIST, COMPUTATIONAL BIOLOGY in San Diego, CA. Your main responsibilities as a SCIENTIST, COMPUTATIONAL BIOLOGY: · Target Antigen Discovery: Lead efforts to identify and validate novel antigen targets for radiopharmaceutical therapy in oncology through integration of multi-omics data, including RNA sequencing, proteomics, and genomics. · Bioinformatics Analysis: Design and implement novel analytical frameworks to process, visualize and interpret high throughput sequencing and multiplex flow cytometry data from pre-clinical experiments, Real-World cohorts and internal clinical trial data to validate pharmacodynamics effects, confirm the mechanism of action, and enable patient enrichment strategies. · Collaboration: Work closely with computational biology colleagues, and engage with cross-functional teams, including discovery, translational, and clinical scientists, to provide bioinformatics expertise and guidance on experimental design. · Interpretation of Results: Generate hypothesis based on the analyses and present findings to both technical and non-technical stakeholders, providing actionable insights to inform radiopharmaceutical discovery and enable data-driven decision-making. · Oncology Expertise: Apply oncology expertise to understand the molecular mechanisms underlying cancer and therapeutic resistance, particularly in relation to radiopharmaceutical therapy. What we are looking for in a SCIENTIST, COMPUTATIONAL BIOLOGY: · PhD in Bioinformatics, Computational Biology, Cancer Biology, or a related field with 3+ of relevant industry experience. · Expertise in bioinformatics tools and software for RNA-seq, proteomics, and other omics data analysis. · Individual contributor role requiring strong background in -omic (DNA, RNA, epigenetic, proteomic) data analysis, biological interpretation and large-scale data analysis, particularly in oncology. · Proficiency in programming languages such as Python, R, and/or Perl, and experience with bioinformatics software and platforms. · Strong experience in statistical modeling and/or machine learning approaches, such as mixed-effects models, predictive modeling, etc. to represent biological concepts. Why Choose R&D Partners? As an employee, you have access to a comprehensive benefits package including: • Medical insurance – PPO, HMO &, • Dental & Vision insurance, • 401k plan, • Employee Assistance Program, • Long-term disability, • Weekly payroll, • Expense reimbursement, • Online timecard approval Pay Scale: $150,708 – $188,392 Dependent on Experience) R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies. R&D Partners is an equal-opportunity employer. Company DescriptionR&D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined staffing experience providing consulting, direct hire & outsourcing solutions with our west coast offices in San Francisco, Redwood City and San Diego, CA and our east coast offices located in Harrisburg, PA and Tampa, FL. The cornerstone of our success: a knowledgeable and experienced recruiting team. Our life sciences recruiters, clinical research recruiters and engineering recruiters are uniquely specialized. After a detailed assessment of our clients’ needs, we can then identify appropriate candidates utilizing our established network of professionals. R&D Partners takes a proactive approach to recruiting, establishing relationships with experienced passive candidates so when the time is right, we can combine our candidates’ talents with our clients’ opportunities.R&D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined staffing experience providing consulting, direct hire & outsourcing solutions with our west coast offices in San Francisco, Redwood City and San Diego, CA and our east coast offices located in Harrisburg, PA and Tampa, FL.\r\n\r\nThe cornerstone of our success: a knowledgeable and experienced recruiting team.\r\n\r\nOur life sciences recruiters, clinical research recruiters and engineering recruiters are uniquely specialized. After a detailed assessment of our clients’ needs, we can then identify appropriate candidates utilizing our established network of professionals. R&D Partners takes a proactive approach to recruiting, establishing relationships with experienced passive candidates so when the time is right, we can combine our candidates’ talents with our clients’ opportunities.

Job DescriptionCompany Description Veolia is a global leader in environmental services, operating across all five continents with nearly 218,000 employees. Specializing in water, energy, and waste management, Veolia designs and implements innovative solutions for decarbonization, depollution, and resource regeneration, supporting communities and industries in their ecological transformation. Within this framework, Water Tech brings together a dedicated team of experienced professionals committed to tackling the world’s most complex challenges related to water scarcity, quality, productivity, and energy. Together, we pursue a shared mission to create a more sustainable future. Job Description Job Summary The Field Service Engineer (FSE) will provide routine to complex field service support for our core Sievers® brand total organic carbon (TOC) analytical instruments and accessories at at customer sites predominantly within San Diego / Southern California and Arizona. Support will include maintenance, verification, validation, repair, and calibration duties as well as troubleshooting operational issues. This position will require residency in the San Diego metropolitan area and within 1-hour drive of an International Airport. This position will occasionally provide field service support for other customers of Sievers Analytical Instruments as needed within Canada and the US. Key Characteristics We are looking for a resourceful person who is self-directed, enjoys working independently, and is attentive to details. An ideal candidate would prefer to organize their own planning, scheduling and confirmation of contiguous services while balancing varying priorities. We are looking for a candidate who would employ a scientific approach to the operation, maintenance, and repair of analytical instrumentation and is proficient at completing daily and weekly administrative responsibilities. Client focus and succinct & timely communication (written and verbal) are key elements for success in this role. We are looking for a candidate that is technically competent and has work experience in technical field support, customer support and experience in ultra-pure water applications or operation of analytical instrumentation in a lab environment. Duties & Responsibilities • Travel to customer sites and perform PM and related services on TOC equipment, • Plan, Schedule and Confirm customer services including coordination of travel and parts shipments for services, • Maintain admin duties, parts inventory, and relevant trainings, • Take customer calls, participate in territory sales rhythm calls, and service team meetings, • Respond to on-demand contract services with 3 or 7 business day response commitments for troubleshooting and repair, • Write clear and concise reports for customers, • Special projects and new hire training as assigned by supervisors, • Work closely with Sales to provide insight into new instrument and new service opportunities as well as upsell service and consumables at existing customer sites based on need, • Ensure compliance with all aspects of safety on the job, including the operation and maintenance of an assigned company vehicle and comply with all Veolia Environmental, Health and Safety (EHS) policies, • Domestic travel 70%Qualifications Knowledge, Skills & Abilities • Strong technical, mathematical and customer service skills, • Able to prioritize various tasks such as service of multiple instruments and administrative duties, • Troubleshooting and problem-solving skills, ability to use processes to find root cause, • General knowledge of electrical equipment, chemistry, and safety, • Vision, manual dexterity, and coordination sufficient to service instruments and handle electrical equipment, • Ability to learn applicable company procedures within a reasonable time from start of employment, • Computer proficiency with a minimum of word processing, spreadsheets, and basic network and data base knowledge, • Ability to use ordinary hand tools, calibrated tools, and analytical instrumentation, as well as handle chemically aggressive fluids, such as acids and bases, • Strong and concise verbal and written communication skills, • Self-motivated, with the ability to drive projects to completion with minimal oversight, • Proven ability to speak effectively before groups and customers, clients, and other employees within the organization, • Ability to meet deadlines and commitments, • Ability to communicate effectively and contribute within a commercial team environment, • Associate degree in a Science, Technical, or Engineering discipline; or equivalent education, • With at least 3 years of work experience in ultra-pure water applications or servicing and/or operating analytical instrumentation in a lab environment Preferred: • Bachelor’s Degree in Chemical Engineering, Chemistry, Biology, Engineering or Physics; or equivalent education, • With at least 1-year work experience in ultra-pure water applications or servicing and/or operating analytical instrumentation in a lab environment Working Conditions • Ability and willingness to work a flexible schedule based on customer needs, • Drive a motor vehicle - significant time each day in the car driving to customer sites, • Air travel required to reach customer destinations and back up support of other areas, • Ability and willingness to travel to customer’s sites requiring overnight stays approximately 30 to 60% of the time, with short notice as required to perform services and to fulfill contractual response time commitments, • Use of laptop and mobile systems, • Regularly work around machines, electrical equipment, chemicals, and within industrial facilities, • Work at a variety of customer sites including outdoor industrial installations, clean rooms and laboratory environments requiring the use of clean suits/smocks, • Perform tasks requiring manual dexterity during tool use, handling small parts, and repair procedures, • Reach with hands and arms, below and above shoulder height, • Stand, sit, stoop, kneel, crouch, or crawl, • Work in industrial environments where background noise may be present, • Regularly lift and/or move up to 30 pounds. Frequently lift and/or move up to 50 pounds, • Close vision, color vision, depth perception, and ability to adjust focus, • Maintain driver’s license and a good driving record Additional Information At Veolia, we realize diverse teams make smarter decisions, deliver better results, and build stronger communities. We’re an organization that champions diversity and inclusion at every rung of the ladder and are proud to be an equal opportunity workplace. Because our people are our greatest assets, we also offer competitive compensation and benefits that include: ● Compensation - The salary range is tied to the market for similarly benchmarked roles. The range is not an absolute, but a guide, and offers will be based on the individual candidate’s knowledge, skills, experience, and market conditions, as well as internal peer equity. Depending upon all the preceding considerations for the final selected individual candidate, the offer may be lower or higher than the stated range:$31 - $37 USD ● Medical, Dental, & Vision Insurance Starting Day 1! ● Life Insurance ● Paid Time Off ● Paid Holidays ● Parental Leave ● 401(k) Plan - 3% default contribution plus matching! ● Flexible Spending & Health Saving Accounts ● AD&D Insurance ● Disability Insurance ● Tuition Reimbursement This position is expected to stay open until September 30, 2025. Please submit your application by this date, to ensure consideration. Disclaimer: The salary, other compensation, and benefits information is accurate as of the date of this posting. The Company reserves the right to modify this information at any time, subject to applicable law. **Applicants are required to be eligible to lawfully work in the U.S. immediately; employer will not sponsor applicants for U.S. work authorization (e.g. H-1B visa) for this opportunity** VWTS does not accept unsolicited resumes from external recruiting firms. All vendors must have a current and fully executed MSA on file before submitting candidates. Any unsolicited resumes and candidate profiles will be deemed the property of VWTS, and no fee will be due. As an inclusive company, Veolia is committed to diversity and gives equal consideration to all applications, without discrimination.

Job Description About Us: At BlossomHill Therapeutics, we are on a mission to redefine precision medicine and make a leap forward in life expectancy and quality of life for patients. Our cancer therapies are exquisitely designed to be potent against cancer drivers and aim to address cancer’s resistance to treatment from multiple angles. Our autoimmune programs seek to tackle difficult challenges to deliver life-changing therapies for patients. Driven by a desire to transcend incremental improvements to existing drugs, we approach drug design from the ground up. Combining human intelligence, creative thinking, and proven drug design expertise, we are dedicated to developing small-molecule masterpieces that have the potential to set new standards for cancer and autoimmune disease treatment. Position Summary: The Executive Director, Translational Medicine & Biomarker Science, reporting to the Chief Medical Officer, will lead the planning and execution of biomarker and companion diagnostic (CDx) strategies to support the company’s oncology drug development programs. This role focuses on integrating translational science into clinical trials by identifying, developing, and operationalizing biomarker strategies that inform patient selection, pharmacodynamic assessments, and clinical decision-making. The ideal candidate will bring deep scientific and operational experience in oncology biomarkers, assay development, and CDx co-development, and will serve as a senior functional leader working closely with cross-functional teams including Clinical Development, Regulatory, Clinical Operations, and external diagnostic partners. This is an onsite position, based in San Diego. Key Responsibilities: • Serve as the biomarker lead on cross-functional clinical development teams, responsible for the design, execution, and interpretation of biomarker strategies across programs., • Develop biomarker and translational research plans that align with clinical development objectives for early stage trials., • Oversee the selection, qualification, and management of biomarker assays and vendors, ensuring fit-for-purpose assay validation and timely data delivery., • In collaboration with Clinical Development and Regulatory Affairs, lead the identification and management of CDx partnerships and associated development plans., • Manage operational aspects of biomarker and CDx execution, including contracting, oversight of external labs, CROs, and diagnostic companies, and ensuring compliance with quality and regulatory standards., • Contribute to the development of clinical study protocols, ICFs, lab manuals, statistical analysis plans (SAPs), and regulatory filings with biomarker and CDx content., • Provide input into regulatory strategy and participate in regulatory interactions (FDA, EMA, PMDA) related to biomarkers and diagnostics., • Support sample management and troubleshooting efforts in collaboration with Clinical Operations and CROs., • Ensure appropriate documentation and procedures are in place to support biomarker sample collection, handling, and analysis across studies., • Stay abreast of advancements in translational oncology, biomarker technologies, and regulatory expectations to inform program strategy and execution.Qualifications:, • Advanced degree (PhD, MD, or equivalent) in molecular biology, oncology, pharmacology, or related field., • 10–15 years of experience in translational science, biomarker development, or clinical assay development, preferably within oncology drug development., • Expertise in EGFR inhibitors and CLK inhibitors strongly preferred., • Proven experience leading biomarker strategies within clinical-stage programs, including direct involvement in assay development and implementation in clinical trials., • Demonstrated experience with CDx development and regulatory submissions, including interactions with regulatory agencies and diagnostic partners., • Deep understanding of GLP/GCP standards, clinical sample handling, assay validation, and quality control requirements., • Strong working knowledge of preanalytical variables, clinical protocol design, and integration of biomarker endpoints into clinical trials., • Effective cross-functional collaborator with strong communication and organizational skills, capable of operating in a matrixed, fast-paced biotech environment., • Experience managing external partners, including diagnostic companies, central labs, and CROs., • Ability to operate both strategically and hands-on to ensure timely, high-quality execution of biomarker activities. AAP/EEO Statement: The company provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. Recruiters and Agencies: BlossomHill Therapeutics does not accept unsolicited referrals or resumes from any source other than directly from candidates. We will not consider unsolicited referrals and/or resumes from vendors including and without limitation, search firms, staffing agencies, fee-based referral services and recruiting agencies. The submission of referrals or resumes by anyone other than a candidate directly to BlossomHills’ employees is strictly prohibited. Unsolicited referrals and resumes sent to BlossomHill Therapeutics are deemed gratuitous, and the company will not be obligated or bound in any way to pay any referral or other fee if a person referred to us from a source other than a candidate is hired.

Job DescriptionSummary: The Senior Research Associate, Protein Sciences will play a key role in advancing our mission to develop novel therapeutics for cardiometabolic diseases. This position will primarily support the expression and purification of therapeutic candidates and assist with molecular cloning efforts, as well as analyze and present data and contribute scientific insights to drive our research forward. The Senior Research Associate will collaborate closely with cross-functional teams to accelerate progress, delivering reproducible, reliable data and solutions that help move promising therapies closer to patients who need them most. • Manage the expression and purification of proteins in mammalian cell systems, supporting multiple teams and molecular biology efforts as needed., • Develop and employ processes to produce endotoxin-free material., • Operate and maintain relevant laboratory equipment including incubators, biosafety cabinets, FPLCs, and other related instruments., • Review and contribute to the creation and revision of SOPs related to expression and purification practices and maintain accurate reporting in an electronic lab notebook system., • Knowledge of mammalian cell transfection techniques, especially lipofection, for CHO and HEK293 cells., • Familiarity with chromatography techniques such as protein A, ion exchange, Ni-NTA, and desalting., • Knowledge of endotoxin-removal procedures and methods for maintaining instrumentation to prevent endotoxin contamination., • Experience with FPLC operation and troubleshooting, particularly using ÄKTA Avant or ÄKTA Pure systems.Experience with molecular biology techniques, including cloning (restriction enzyme digestion/ligation, Golden Gate assembly, or Gibson assembly), bacterial transformation and culture, and DNA preparation and characterization., • Strong analytical and problem-solving skills with attention to detail., • Excellent organizational and time-management abilities., • Strong verbal and written communication skills.Ability to work both independently and collaboratively in a fast-paced environment.

Job Description Overview Ansible Government Solutions, LLC (Ansible) is currently recruiting Medical Technologists to support the VA Medical Center located at 3350 La Jolla Village Dr, San Diego, CA 92161. Services will be delivered to both the Anatomic Pathology and Clinical Pathology divisions of the facility. Exceptional compensation packages with full benefits are available. Ansible Government Solutions, LLC (Ansible) is a Service-Disabled Veteran-Owned Small Business (SDVOSB) providing Federal customers with solutions in many arenas. Our customers face wide-ranging challenges in the fields of national security, health care, and information technology. To address these challenges, we employ intelligent and committed staff who take care of our customers’ success as if it is their own. Responsibilities • Rotate on a regular basis through the areas in which they have been trained and are competent, • Perform a broad range of laboratory procedures in Blood Bank., • Perform advanced and complex laboratory procedures, recognizing deviation from expected results, analyzing and correcting problems using scientific principles, • Recognize and communicate pre-defined critical results affecting patient care, • Maintain the optimal functioning of laboratory equipment and keep appropriate records for documentation; operate, calibrate, identify malfunctions, repair and perform preventive maintenance of laboratory analyzers, • Perform and document quality control, quality assurance and corrective actions related to test performance using sound statistical principles and theories of performance improvement, • Enter and verify laboratory results in the computer system; recognize deviations from expected results, analyze and correct problems using scientific principles, • Accredited Bachelors degree including 16 semester hours in biological science (one course in microbiology), 16 semester hours in chemistry (one course in organic or biochemistry), and one course in mathematics AND two (2) years of post-certification clinical laboratory experience within the last ten (10) years as a certified Medical Laboratory Technician (ASCP-BOC), • A minimum of one (1) year of Medical Technologist experience within the last three (3) years, • Demonstrated knowledge of laboratory medicine techniques and practices, • Demonstrated education and clinical training in the practice of laboratory medicine All candidates must be able to: • Sit, stand, walk, lift, squat, bend, twist, and reach above shoulders during the work shift, • Lift up to 50 lbs from floor to waist, • Lift up to 20 lbs, • Carry up to 40 lbs a reasonable distance Powered by JazzHR DgRdMIsBZh

Job DescriptionDescription: An excellent opportunity exists to work for a government contractor with competitive compensation and work-life balance. Posterity Group is seeking experienced Dental Assistant at the Naval Medical Center San Diego. • Certificate or associate degree as a dental assistant/technician from a program accredited by the Commission on Dental Accreditation (CODA) of the American Dental Association (ADA) and 12 months experience within the preceding 36 months., • Certification from a military dental technician or dental assistant school and 12 months experience within the preceding 36 months., • Certification from a Red Cross Dental Assistant course and 12 months experience within the preceding 36 months., • 36 months experience within the preceding 60 months as a dental assistant in a private practice or a military clinic., • Membership in good standing with the American Association of Dental Assistants with required continuing education and 12 months experience within the preceding 36 months., • Graduation from a state accredited program for dental assistants or dental technology within the preceding 12 months., • All training must have included a course in radiation physics; radiation biology; radiation health, safety, and protection; X-ray films and radiographic film quality; radiographic techniques; darkroom and processing techniques; film mounting; and digital radiographic processing techniques. Requirements:, • Performs duties in providing assistance in one or more phases of complex/difficult restorative, prosthodontic, oral surgical, endodontic, or periodontal treatment. Receives and schedules patients for treatment., • Obtains and records related medical history of patient. Charts examination and treatment information. Records information on prescriptions., • Sterilizes instruments, materials, and equipment; prepares surgical trays. Maintains dental equipment in a clean and operative condition., • Assists dentist at chair side. Performs intra-oral procedures as directed by dentist. Takes preliminary impressions for study models, removes sutures, places and removes rubber dams, perio-packs, matrix bands, and wedges., • Relays dentist’s instructions to patient for post-treatment care. Instructs patient in proper dental techniques, care of appliances, and causes of dental decay., • Operates dental X-ray equipment to take intra and extra oral radiographs. Maintains, cleans, and performs minor repairs on X-ray equipment and materials., • Pours and trims models from impressions and constructs custom impression trays. Maintains a variety of recurring reports related to dental activities.

Job DescriptionSr. Principal Scientist / Associate Director – Antibody Engineering Location: San Diego, CA Employment Type: Full-time Hiring Company: BioPhase (on behalf of our client) Pay: $170,000–$190,000 base + bonus; stock options Hours: Monday–Friday, full-time (no overtime) Job Description: We’re seeking a hands-on scientific leader to head Protein/Antibody Engineering. You’ll guide strategy and execution from hit discovery through optimization to development candidate, manage a small team, and partner closely with cross-functional groups to advance novel biologics. Essential Duties and Responsibilities: • Serve as subject-matter expert for protein/antibody engineering, formatting, and structure–function hypotheses., • Lead, mentor, and develop protein engineering scientists; provide technical oversight., • Act as project lead to deliver milestones across discovery programs., • Collaborate with biology, computational, and development teams to progress hits into developable candidates., • Design/build antibody & protein combinatorial libraries; plan and run engineering campaigns., • Drive continuous improvement of lab workflows and data practices., • Oversee curation/aggregation of experimental & in-silico data to inform predictive models., • MS/PhD in Biochemistry, Chemistry, or related field with 7+ years biopharma experience., • Deep knowledge of protein structure, interactions, and physicochemical properties., • Proven people leadership and experience managing scientists., • Track record leading cross-functional programs from target validation through optimization to candidate nomination., • Advanced understanding of multiple antibody formats (mAbs, bi/multispecifics, scFv, sdAbs, etc.)., • Extensive hands-on experience in antibody/protein engineering (humanization, liability removal, optimization)., • Familiarity with developability assessments (solubility, stability, manufacturability) and using them to guide design., • Experience with plate-based assay development & high-throughput workflows., • Engineering of small proteins/enzymes.

Job DescriptionSalary: $110,000 - $120,000/year Job Overview BPS Bioscience Inc. is a leading provider of recombinant proteins, assay kits, and recombinant cell lines for drug discovery. We are seeking an exceptional scientist, with a strong background in enzymology, enzyme kinetics, protein/protein interactions, and fluorescence and luminescence-based assays. We are seeking a highly skilled Senior Scientist I with deep expertise in antibody generation to join our Molecular and Cellular Biology team. This position plays a critical role in driving research and development efforts, with a primary focus on the design, expression, engineering for multiple targets, purification, and optimization of antibodies, including phage display, single B cell isolation, humanization, and stable cell line generation. The ideal candidate will have strong industry experience and be adept at independently designing and executing experiments at a high standard. Responsibilities: • Lead and execute projects related to antibody generation, including:, • Antibody design and engineering (e.g., humanization, affinity maturation, bispecific antibody), • Molecular cloning and vector design, • Transient and stable expression in mammalian system, • Antibody purification using affinity chromatography and other techniques, • Develop and optimize stable cell lines for antibody production, • Utilize fermentation systems for antibody expression (small- to mid-scale), • Evaluate and integrate new technologies to enhance R&D capabilities, • Participate in team meetings, project planning, and cross-functional collaborations, • Design and perform cell-based functional assays to characterize antibody activity, • Present research findings internally and externally, including at scientific conferences, • Maintain rigorous documentation and ensure high standards of data integrity, • Maintaining excellent working relationships with partners throughout the company., • Maintaining updated and well-organized lab notebooks., • Other tasks and duties as assigned. Requirements: • A Ph.D. degree in Molecular Biology, Cell Biology required., • Minimum 3 - 5 years industry experience focused on antibody generation required, • The candidate must have proven experience performing enzyme kinetics and assay optimization., • Proven track record in antibody discovery and development, including engineering and functional validation, • Extensive experience with phage display, mammalian cell culture, sterile technique, and molecular biology methods, • Proficiency in downstream processing including protein purification and analytical characterization, • Strong problem-solving skills and ability to manage multiple projects in parallel, • Excellent written and verbal communication skills, • Team-oriented with a collaborative mindset and attention to detail Benefits! • 401k with 4% company match, • Medical/Dental/Vision health insurance plans, • Vacation and paid holidays, • Companywide lunches provided quarterly BPS Bioscience is an equal opportunity employer, without regard to race, color, religion, age, gender, sexual orientation, disability, or any other characteristic protected by applicable law.

Job DescriptionJob Title: Senior Platform Applications Scientist Reports to: VP, Translational Research FLSA: Exempt Location: San Mateo/San Diego Position Summary: At ClearNote Health, we combine novel epigenomic technologies with our innovative machine learning architecture to tackle the most urgent challenges in cancer care. We are looking for a highly motivated and experienced scientist with similar passion to join our mission to develop next-generation non-invasive cancer diagnostics for better patient outcomes. As an accomplished scientist with skill in design and execution of complex multidisciplinary projects toward molecular diagnostic tests in the treatment of cancer, you will contribute to the design and management of projects that employ the company’s novel platform technologies in drug development in collaboration with pharma partners. The projects will enable the company to formulate clinical questions that contribute to the care of cancer patients. Responsibilities: • Lead relationships with external collaborators and pharma partners to drive projects from inception to completion., • Lead and manage research projects with pharma partners that address fundamental questions using our state-of-the-art platform technology in diagnostic and therapeutic areas in oncology., • Ensure high data quality and the requisite scientific background and knowledge to navigate the complexity of experimental design and interpretation., • Build a continually expanding knowledge base in cancer biology, biomarker discovery and development., • Work in a collaborative and project-oriented manner with interdisciplinary teams composed of laboratory scientists, data scientists and bioinfomaticians as well as commercial and marketing personnel, and ensure that members contribute to their highest potential., • Ability to manage cross-functional projects and timelines., • Support, nurture, and help close sales opportunities., • Role requires 10% travel., • Exemplify our core values:, • Put Patients First: Focused on serving patients and their support system, we direct all our efforts toward the area of greatest impact by discovering and building with speed, excellence, and purpose., • Redefine the Possible: We are daring, imaginative, and focused in our pursuit of the next big idea. We take calculated risks to grow our business and improve patients’ lives., • Together We Win: We encourage and challenge each other to achieve the greatest positive impact on those we serve: our customers, patients, colleagues, and stakeholders.Requirements:, • M.D./Ph.D. or Ph.D. in Oncology, Cancer Biology, Epigenetics and Genomics or related field with 6+ years’ relevant experience in positions of increasing responsibilities with 3-6 years of in industry., • Experience in leading and working in teams with a history of successful project management., • Experience in the field of oncology and its underlying biology, along with genomics and epigenomics expertise, as demonstrated by publications, involving impactful tools or data sets as well as presentations at international conferences., • Understanding existing large data sets and modern tools in cancer genomics for processing and analysis of primary data. Proficiency in programming languages such as R or python is a plus., • Experience in biomarker development or molecular diagnostics in industry is strongly preferred., • Experience with experimental design in population based clinical studies., • An understanding of experimental limitations of next generation sequencing experiments as applied broadly in cancer., • Demonstrated ability to apply these skills to uncover new biological insights., • Excellent interpersonal, teaming, written and spoken communication skills.Individual compensation is determined based on several factors, including job-relevant skills, expertise, and experience; applicable education or training; a demonstrated track record of exceeding expectations; and geographic location. The typical salary range for this position is estimated at $126,000–$164,000 for candidates based in the San Francisco or San Diego metro areas. Exceptions to this range may occur from time to time based on the depth of technical experience and other job-relevant qualifications.Come join us in addressing large healthcare needs through precision epigenomic medicine! Come join us in addressing large healthcare needs through precision epigenomic medicine! ClearNote Health is an exciting life science company that is reinventing non-invasive molecular diagnostic testing using next generation epigenomic technologies. We are passionate and dedicated to discovering and developing medicines that will make a significant difference in cancer and other epigenomic-driven diseases. Our technologies provide novel insight and quantitation of human health and disease, with our focus on precision medicine applications improving both clinical and health system outcomes. Our company was founded based on pioneering work in the Stanford laboratory of Stephen Quake, with advisors from Stanford and UCSF. We look for extraordinary lifelong learners with a passion and growth mindset for these areas, and for combining biological ingenuity with AI and data analysis. Led by a team with decades of experience bringing products from concept to market, we are an equal opportunity employer and value diversity at our company. We provide generous benefits to all employees including stock options. We are building a world-class company, based in San Diego and San Mateo. Our commitment to Diversity, Equity, Inclusion, and Belonging: We celebrate diversity in perspectives and backgrounds, and this is reflected in our innovation, our mission, and values. Our differences make us unique, help us innovate, and allow us to persevere. We strive to achieve representation and inclusion and redefine the possible in patients living longer lives. Powered by JazzHR ZAHKsbMaGt

Job DescriptionAbout San Diego BioMed: San Diego BioMed (SDB) is a nonprofit biomedical research institute located in San Diego, California. The mission of SDB is to conduct fundamental biomedical research to better understand human disease, and to use this information to contribute to the treatment and prevention of diabetes, cancer, neurological disease, HIV infection and complications of chronic disease. The Principal Investigators at SDB are accomplished scientists and well-known and recognized in their areas of expertise. SDB is located in the heart of San Diego’s science park area, which is part of the largest and most concentrated centers of science, engineering, and medicine in the United States. Further information on SDB can be found at . Position and Project Overview: San Diego BioMed (SDB) is seeking a full-time or part-time, focused and detail-oriented Research Associate to work in the laboratory of one of its Professors/Principal Investigators. The lab is focused on chromatin 3D organization/replication timing using pluripotent stem cells/in vitro differentiation/genome editing with CRISPR/genomics. The major goals of the lab are to understand the mechanisms regulating replication timing during cell fate transitions. The Research Associate will perform a variety of hands-on research duties in the laboratory. Project details: Identifying the DNA sequence requirements of ERCEs (early replication Control Elements) using a high throughput insertion assay. Job Duties: • Perform pluripotent stem cell culture and engineering, screening by PCR, • Prepare NGS libraries (mainly Repli-seq, Bru-seq, more as needed), • Update lab inventories (supplies, chemicals, reagents) and ordering consumables., • Draft and update lab protocols., • Monitor and maintain lab equipment, arrange repair if needed, • Write up experiments (date, description and inferences) in a timely manner., • Assist PI with regulatory documents, • Perform other duties as requiredMinimum Qualifications:, • B.S. or M.S. degree in or related to the areas of biomedical sciences, • Candidates with a Ph.D. in a related area are also encouraged to apply, • Minimum 3 years of experience., • Previous experience in mammalian cell culture and molecular biology, • Familiarity with LINUX, • Self-motivated and independent problem solving are important Benefits: San Diego BioMed offers a competitive benefits package, including medical, dental, vision, life insurance, long-term disability, paid time off, and a generous employer match to the retirement plan. The work environment at San Diego BioMed is one that fosters and promotes collaboration and inclusivity. SDBRI is committed to a policy of equal employment opportunity in regard to recruiting, hiring, training and promoting the most qualified individuals, without regard to race, color, creed, religion, sex, sexual orientation, gender, gender identity and expression, marital status, age, registered domestic partner status, national origin or ancestry, physical or mental disability, age, disability, protected veteran status, medical condition including genetic characteristics, or any other protected status as designed by federal, state, or local law. Powered by JazzHR 7kg75PsMIu

Job Description VTI Life Sciences (VTI) seeks forward-thinking and ambitious engineers looking to accelerate their careers in the pharmaceutical, biotechnology, and medical device industries. We offer an opportunity to help support our teams of industry subject matter experts and thought leaders while consulting with some of the biggest companies in the Life Sciences industries. We are looking to staff a highly motivated Validation Specialist/ Engineer 1 responsible for delivering commissioning, qualification, and validation (CQV) services related to equipment, instruments, and systems for clients in the biotech/pharmaceutical / medical device industry. This field service role will be based out of the Greater Los Angeles area and requires potentially full-time travel throughout California and the US. This role primarily involves performing qualification (IQ/OQ/PQ) and temperature mapping protocols independently, analyzing test results, and preparing technical reports. As a VTI employee, you will continue to learn and implement industry-standard methods for CQV (ISPE Baseline Guide, ASTM E2500) and temperature mapping in a GxP (good practices) regulated environment. As you progress, you will have the opportunity to support future projects of increasing complexity and specialization as you navigate your career in this always-in-demand field. Qualifications: • Bachelor's degree or higher in Engineering, Life Sciences, or related discipline (Mechanical Eng., Chemical Eng., Chemistry, Biology, etc.), • Previous experience with CTU temperature mapping, thermocouple prep, handling, and calibration., • Previous experience with Autoclave Qualification., • Experience with Kaye Validators and data loggers is a huge plus., • Previous experience with CQV, including qualification protocol (IQ/OQ/PQ) generation, execution, and reporting is a plus., • Previous experience in a cGMP/FDA-regulated manufacturing environment is a plus., • Must be proficient with/ Microsoft Office, including Word, Excel, PowerPoint, etc., • Must have technical writing, review, and analytical skills in addition to strong verbal communication and presentation skills, • Must have a strong ability to organize and manage multiple tasks in a fast-paced environment with changing schedules VTI Life Sciences strives to maintain and inspire professional excellence by providing Commissioning, Qualification, Quality Engineering, Automation, and Validation Services to the Pharmaceutical, Biotechnology, Biologics, and Medical Device industries. VTI offers professional development, training, competitive compensation, excellent benefits, 401K, plus a stimulating and collaborative work environment. We are committed to providing exciting career opportunities in a work environment that values trust, respect, openness, teamwork, creative talent, enthusiasm, and diligence. As one of the leading global Commissioning, Qualification, and Validation Services organizations, VTI always seeks innovative, talented, and experienced validation professionals for our multinational and global offices. We offer some of the industry's best salary and benefit packages for our full-time/permanent employees and competitive hourly pay for our contractors. Powered by JazzHR gnGgpKiGSQ

Job DescriptionDescription: We are seeking a dynamic and results-driven Business Development Manager to drive growth and expand our market presence. This strategic role is responsible for managing and expanding current business, identifying new opportunities within existing accounts, and pursuing and closing new business within the assigned territory. The ideal candidate will be a proactive sales leader who thrives in a fast-paced environment, builds strong customer relationships, and develops targeted sales strategies that align with company objectives. Territory: Southwest Region (South CA, South NV, AZ, NM, CO, HI and UT) Preferred Locations: Greater San Diego Area Job Responsibilities: • Strategic Business Growth: Develops and implements a comprehensive business plan to drive revenue growth and expand market share., • Account Leadership: Builds and maintains strategic account plans, collaborates with global account teams, and provides data-driven insights on competitor activities and market trends., • High-Impact Sales Execution: Consistently meets or exceeds sales targets by optimizing account management strategies and uncovering new opportunities., • Market Expansion & Lead Generation: Identifies, nurtures, and converts high-value prospects into long-term customers. Develops targeted engagement strategies for key accounts., • Executive-Level Relationship Management: Engages and influences key decision-makers at all levels, from bench scientists to C-suite executives, to position the company as a preferred partner., • Technical & Solution-Based Selling: Effectively presents the capabilities and value of MaxCyte technology, aligning solutions with customer needs to drive long-term partnerships., • Customer & Competitive Intelligence: Conducts in-depth account research to understand customer priorities, financial standing, and competitive positioning., • Sales Forecasting & CRM Excellence: Provides accurate sales forecasts, maintains an up-to-date pipeline in CRM, and ensures thorough opportunity tracking and reporting., • Strategic Product Demonstrations: Leads high-impact presentations and product demonstrations, working closely with technical teams to showcase differentiated value., • Cross-Functional Collaboration: Partners with internal stakeholders, including marketing, applications, and product teams, to refine sales strategies and support customer success., • Compliance & Leadership: Adheres to all company policies related to health, safety, and the environment while mentoring junior sales professionals.Requirements:, • Education & Experience: BS in Life Sciences or a related field with a minimum of 10 years of direct sales experience in companies that develop, market, and sell life science tools to biotechnology, pharmaceutical, and research markets., • Capital Equipment Sales Expertise: Extensive experience selling capital equipment ($100K+) to pharmaceutical and biotech accounts, with a proven track record of success., • Advanced Sales & Communication Skills: Strong ability to develop trust-based relationships and sell at all levels within customer organizations, from technical end-users to C-suite executives. Industry Network & Technical Acumen: Established relationships within the fields of protein production, cell therapy, immunology, cell biology, high-throughput screening, and high-content screening., • Sales Process Mastery: Deep understanding of the sales process with the ability to drive opportunities through the pipeline efficiently and manage complex sales cycles., • Scientific & Technical Expertise: Strong knowledge of Cell and Gene therapy, cell line development and manufacturing, immunology, and cell-based assays, with an understanding of transfection techniques and technologies., • Entrepreneurial Mindset: Proven ability to thrive in an entrepreneurial, high-growth environment, demonstrating strategic thinking, problem-solving, and self-motivation., • Customer-Centric Leadership: Builds and maintains strong customer relationships, demonstrating passion for the company’s mission and solutions., • Travel Requirement: Ability to travel approximately 50% (domestic and international) to engage customers, drive business growth, and expand strategic partnerships. The compensation package for this role includes a base salary of up to $160,000 (depending on experience), commission, and equity. MaxCyte also offers a comprehensive benefits package including health, dental, vision, life, and disability insurance and generous time off. MaxCyte is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status. PIbd92a7d9beb3-25405-38058134

Job DescriptionRegulatory Affairs ManagerLocation: San Diego, CA (Onsite) Salary Range: $145,000 - $165,000Job SummaryBioPhase is seeking a Regulatory Affairs Manager to lead regulatory strategy and compliance for in vitro diagnostic (IVD) products. This role oversees regulatory submissions, market authorizations, and agency communications, ensuring compliance with FDA, EU IVDR, and global regulations. The ideal candidate will collaborate cross-functionally and drive regulatory excellence.Responsibilities • Develop and execute global regulatory strategies for IVD products., • Lead preparation of 510(k), IVDR Technical Documentation, and other regulatory submissions., • Manage regulatory assessments for product changes and compliance., • Collaborate with R&D, Quality, Manufacturing, and Marketing teams., • Mentor and lead a team of regulatory professionals., • Monitor global regulatory trends and implement best practices., • Support regulatory inspections and audits.Qualifications, • Bachelor’s degree in Bioengineering, Biochemistry, Molecular Biology, or related field (Advanced degree preferred)., • 8+ years in Regulatory Affairs, with 5+ years in IVD regulatory roles., • Experience securing approvals in US, EU IVDR, Canada, Australia, etc., • Strong leadership and cross-functional collaboration skills., • Proficiency in regulatory submission tools and Microsoft Office Suite.Work Environment & Travel, • Onsite in San Diego, CA., • Limited travel (<10%).

Job Description Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. The Position Arrowhead Pharmaceuticals is seeking a talented and motivated Scientist or Senior Scientist in Computational Drug Design to join our interdisciplinary drug discovery team. This role is ideal for a creative, independent thinker with strong technical skills in machine learning and a passion for applying computational approaches to advance next-generation therapeutics. The successful candidate will contribute to the design and optimization of novel antibody-siRNA conjugates using cutting-edge AI/ML methodologies. Responsibilities • Develop and curate large biological datasets by integrating internal and publicly available data sources., • Design, train, and apply predictive models for antibody-siRNA conjugate drug design., • Apply AI techniques to extract insights and generate testable biological hypotheses from model outputs., • Monitor and critically assess emerging developments in AI/ML for therapeutic discovery., • Ph.D. in Computational Chemistry, Computational Biology, Bioinformatics, Computer Science, or a related discipline., • Strong programming skills in Python (or equivalent), with experience using common scientific libraries and proficiency in UNIX-based environments., • Practical experience with deep learning frameworks such as TensorFlow, PyTorch, or JAX., • Proven experience applying machine learning to solve complex biological or chemical problems., • Hands-on experience in RNA and/or protein structure prediction and relevant in silico design tools., • A strong track record of scientific impact as evidenced by publications, conference presentations, or patents. All applicants must have authorization to work in the US for a company. California Applicant Privacy Policy

Job Description Job Summary The Associate Scientist, Analytical Development will play a key role in developing and executing mass spectrometry methods to support research and clinical programs. This is a hands-on laboratory position involving experimental design, data analysis, and interpretation to guide decision-making across cross-functional teams. The individual will contribute to analytical method development, qualification, and troubleshooting, while maintaining a strong focus on data quality, innovation, and compliance. Key Responsibilities * Design and perform experiments to develop, optimize, and qualify analytical methods for release, stability, and extended characterization testing. * Analyze experimental data, interpret results, and propose next steps to improve methods or resolve analytical challenges. * Implement novel analytical and mass spectrometry techniques for characterization of biologics and complex molecules. * Document experiments in electronic laboratory notebooks and prepare detailed technical reports summarizing findings. * Present data and updates regularly in team and project meetings. * Ensure all work adheres to regulatory standards and internal policies, including FDA, EMA, ICH, and GMP requirements. * Collaborate with cross-functional teams to support research, development, and technical operations initiatives. * Contribute to a culture of innovation, teamwork, and scientific excellence. Qualifications * Masters degree in Chemistry, Biology, or Pharmaceutical Sciences, or a Bachelors degree with at least 4 years of relevant experience in mass spectrometry analysis of biologics. * Hands-on experience with LC-MS/MS, HPLC, CE, and related analytical techniques. * Strong knowledge of antibody and/or oligonucleotide analytical characterization. * Demonstrated ability to analyze complex data and solve technical problems independently. * Excellent communication, organizational, and interpersonal skills. * Ability to work collaboratively in a fast-paced, multidisciplinary environment while managing multiple priorities effectively.

Job Description WHAT WE DO: Calidi Biotherapeutics is a clinical-stage immuno-oncology company with proprietary technology that is revolutionizing the utilization of oncolytic viruses through an allogeneic cell-based delivery system. Calidi Biotherapeutics is advancing this potent stem cell and oncolytic virus combination for use in multiple difficult-to-treat oncology indications. Our team is also developing a universal cell delivery system to protect, amplify and potentiate oncolytic viruses currently in development. Job Overview/Summary: The IN VITRO Research Associate, performs research and/or development in collaboration with others for projects. Makes detailed observations, analyzes data and interprets results. Investigates, creates and develops new methods and technologies for project advancement. Essential Duties and Responsibilities: • Generate immunophenotyping and immune cell functional data using techniques such as multicolor flow cytometry, ELISA, and xCELLigence RTCA., • Isolate protein, DNA, and RNA from cell cultures and tissues; perform gene and protein analysis using qPCR and Western blot., • Maintain primary and established cell lines to support in vivo studies., • Assist with general cell culture for the production of oncolytic viruses, including herpes simplex virus, vaccinia virus, and/or adenovirus., • Contribute to the generation of recombinant therapeutic viruses., • Support the in vivo team as needed, including animal handling and sample collection., • Analyze and organize experimental data with strong attention to detail., • Assist with laboratory maintenance, inventory, and cleaning tasks., • Adhere to EH&S guidelines, participate in mandatory safety training, and follow SOPs to ensure study integrity and compliance., • Perform other duties as assigned. Skills/Qualifications: • 2+ years of experience in a biotechnology company with broad knowledge and experience in cell and molecular biology methods; Immuno-Oncology field is preferred., • Experience with mamallan cell culture is required., • Experience in immune cell based assay (ELISA, MSD, cytotoxicity assays) is required. Strong hands-on experience in acquiring and analyzing flow cytometry data (multi-parameter flow cytometry, intracellular, extracellular staining, flowjo analysis) is highly desirable., • Experience with mouse handling, including restraint, injection (IP, IV, SC), and tissue collection is highly desirable., • Experience in a range of in vitro cellular/molelecular biology techniques (cell culture, cloning, qPCR, Western blot, immunohistochemistry, microscopy) is preferred., • Excellent data organization, analysis, and troubleshooting skills using electronic lab notebook., • Dedication to working in a team-oriented environment to contribute to shared project., • Strong work ethic, self-motivation, and ability to multi-task in a fast-paced work environment., • Strong knowledge of MS Word, Outlook, PowerPoint, Excel, Graphad Prism, Flowjo. Education, Certificates, Licenses, Registrations: • B.S. or higher in life science, or related field Mathematical Skills: • Ability to work with mathematical concepts such as calculation of dilutions and statistical analyses., • Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations. REASONING ABILITY: • Ability to define problems, collect data, establish facts, and draw valid conclusions. Language Skills: • Excellent communication skills with ability to effectively communicate with other research teams, • Ability to read and understand technical procedures, • Ability to write protocols and reports, • Ability to effectively present data and respond to questions from co-workers The Perks: • Breakroom snacks and beverages, • Competitive Total Rewards package (Medical, Dental, Vision) offered to full-time employees, • Stock options Work Location: Calidi Biotherapeutics employment provides the opportunity to work in beautiful San Diego, California only minutes from the nearest beach. EOE and Accommodation: We value diversity and are proud to be an Equal Opportunity and Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law. Calidi Biotherapeutics provides reasonable accommodation in job application procedures for qualified individuals with disabilities and disabled veterans. If you need accommodation in connection with the recruiting process due to a disability, you may include this information in your cover letter. If you are selected to interview for a position, you may also request an accommodation with our team directly. Notice to Agency and Search Firm Representatives Calidi Biotherapeutics is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Calidi Biotherapeutics employee by a third-party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Calidi Biotherapeutics. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. EMPLOYER’S RIGHTS: This job description does not list all the duties of the job. You may be asked by supervisors or managers to perform other duties. You will be evaluated in part based upon your performance of the tasks listed in this job description. The employer has the right to revise this job description at any time. The job description is not a contract for employment, and either you or the employer may terminate employment at any time, for any reason.

Job DescriptionCompany Description Consider joining Lancaster Laboratories where people are the most important element in our chemistry. Celebrating 50 years of service, Lancaster Laboratories is a leading contract lab providing testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide. Job Description • Perform cell and molecular biology techniques, including tissue culture, nucleic acid isolation, RT-qPCR, and next-generation sequencing (NGS)., • Design, execute, troubleshoot, and optimize assay workflows to enhance experimental performance and reliability., • Analyze primary and secondary NGS sequencing metrics to support research projects., • Analyze, interpret data and share results with stakeholders in one-on-one meetings and group settings., • Collaborate with bioinformatics and translational team members to generate datasets and identify biomarkers supporting translational medicine, • Develop and run cell-based assays to characterize drug target pathway activity or PD biomarkers in primary cells or cell lines, • Maintain thorough, accurate and complete records of experiments performedQualifications, • Strong and effective communication skills in one-on-one conversations and in group settings, • Strong problem-solving and organizational skills, • Experience with NGS platforms (Illumina preferred), library prep and analyzing sequencing metrics, • Experience in developing and running transcriptomics experiments (bulk and single cell RNA seq) and library preparation for genomic and transcriptomic sequencing., • Experience using cell and molecular biology techniques, including tissue culture, nucleic acid isolation, RT-qPCR, cell culture skills including cell lines and primary cells, • Experience developing ex-vivo cell-based assays to assess immune responses from human whole blood, PBMCs, and various immune cell subsets, • BS or MS in immunology, cell biology, or related biomedical science, • 3-5 years of experience in academia and/or industry Additional Information What we offer: • Excellent full time benefits including comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match, • Paid vacation and holidays Position is full-time, 8am - 5pm with occasional overtime required. Eurofins Lancaster Laboratories Professional Scientific Services® (PSS) is a global, award-winning insourcing solution that places our people at our clients’ site dedicated to running and managing laboratory services while eliminating headcount, co-employment and project-management worries. We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment. Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description Job Description: We are seeking a highly motivated and qualified individual to join our Discovery Biology Department as a Senior Scientist I and work as part of a team to drive success. The Senior Scientist I will support ongoing RNA-based drug discovery projects in several therapeutic areas. The successful candidate will have experience in neuroscience drug discovery and a deep understanding of human neurobiological processes that drive CNS disease pathophysiology. The Senior Scientist I will employ a variety of in vivo, ex vivo, and in vitro techniques to advance oligonucleotide therapeutics for CNS indications. Essential Responsibilities: • Carry out assigned laboratory functions applying knowledge and skill in an accurate, timely manner., • Support the establishment and maintenance of primary and IPSC-derived neuronal cell models., • Support in vivo studies by performing basic animal handling and specialized CNS techniques (e.g. intracerebroventricular and intrathecal injection), • Perform brain and spinal cord dissections and tissue processing. Collect bodily fluids, e.g. blood and cerebrospinal fluid., • Implement multiple state-of-the-art techniques in molecular biology, biochemistry, and microscopy to determine drug distribution, efficacy, safety, and mechanism of action., • Critically evaluate, interpret, summarize, and present data to internal project teams and leadership., • Maintain a current knowledge of relevant literature, competitive landscape, and methodologies specific to oligonucleotide-based therapeutics targeting CNS disorders., • Contribute to the preparation of research reports and presentations for internal project teams, leadership team, and external audience., • Maintain updated and well-organized lab notebooks., • Establish and maintain excellent working relationships with critical collaborative partners throughout the company., • Execute daily laboratory operations with an approach designed to minimize risks and hazard waste streams to carry out assignments., • Maintain all appropriate corporate standards for facility safety and hazardous material management. Reasonable accommodation(s) may be made to enable qualified individuals with disabilities to perform the essential functions of a job, on a case-by-case basis. On-Site Protocol: Physical presence at the ADARx Pharmaceuticals worksite is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture. Qualifications: • Ph.D. in Neuroscience, Pharmacology, or related scientific discipline, • 3+ years post-doctoral or biotech/pharmaceutical industry experience in neuroscience research and drug discovery., • In-depth knowledge in the field of neuroscience, CNS disease and therapeutic modalities., • Expertise in the rodent stereotaxic surgery techniques including intracerebroventricular and intrathecal injection, • Expertise in rodent brain and spinal cord dissection., • Experience with tissue processing, embedding and microtomy of brain tissues, fixation and immunohistochemistry., • Experience in gene expression analysis using qPCR and protein analysis techniques., • Broad knowledge of scientific experience with track record of scientific achievement demonstrated by peer-reviewed publications., • Understanding of project timelines and deliverables and plans/coordinate project work accordingly with departmental, functional, and external stakeholders., • Strong problem-solving skills and a proactive attitude towards exploring new approaches., • Excellent written and verbal communication skills and effective presentation of complex scientific data to cross-functional and senior management teams are essential for this role., • Ability to work as part of a team with a drive to partner effectively with internal and external leaders., • Experience with oligonucleotide-based therapeutics is highly desirable., • Prior experience in biotech/pharmaceutical industry a plus., • Experience in primary neuronal cell cultures and human iPSC-derived neural cells is a plus., • Experience in collection of cerebrospinal fluid samples is a plus., • Must be able to work independently as well in cross-functional team settings with supervision as needed., • Adaptable / Flexible - willing and able to adjust to multiple demands and shifting priorities as well as an ability to meet day-to-day challenges with confidence and professionalism., • This is a full-time position, Monday-Friday, occasional overtime., • Pay is commensurate with experience., • Equity-based compensation, • Performance-based bonuses, • 401(k) with Company Match, • Medical, Dental, Vision, • Flexible Spending Account, • Life Insurance, • Employee Assistance Program, • Employee Discounts, • Paid Vacation, • Paid Holidays, • United States (Required), • Background Check Company Overview: ADARx Pharmaceuticals, Inc., (the “Company” or “ADARx”) located in San Diego, is a clinical stage biotechnology company committed to turning cutting-edge science into life-saving therapeutics. ADARx has developed proprietary RNA targeting platforms and technology for silencing or editing target mRNA. ADARx has a growing pipeline of RNA targeting therapeutics for treating diseases across a range of therapeutic areas including genetic, cardiometabolic, complement-mediated diseases and central nervous system. ADARx currently has multiple active programs in development with the lead candidate in the clinic. We are well-financed by a syndicate of renowned VC firms. ADARx Pharmaceuticals is an EEO employer committed to an exciting, diverse, and enriching work environment. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. Disclosure Statement: • The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position., • Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations., • The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual target bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, type and length of experience within the industry, and other job-related factors permitted by law., • Total Compensation includes base salary; benefits: medical, vision, and dental insurance; life insurance; 401(k) matching program; paid time off; paid holidays; Employee Assistance Program; and other employee benefits. This role may also be eligible for short-term or long-term incentive compensation, including but not limited to cash bonuses., • Following a conditional offer of employment, satisfactory completion of a background check (including criminal records check) is required prior to beginning employment. Any offer of employment may be rescinded if the background check reveals disqualifying information, and/or it is discovered that the candidate knowingly withheld or falsified information. Failure to satisfactorily complete the background check may affect the continued employment of a current NAI employee who was conditionally offered the position.

Job Description Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. The Position Arrowhead is seeking a highly motivated biologist to join our growing CNS in vivo team within the Research Department at our San Diego site. The successful candidate will be joining a team dedicated to discovering, developing and translating novel drug targets. Responsibilities • Perform in vivo studies and ex vivo analysis to facilitate drug discovery and development in various diseases, • Establish new preclinical animal disease models, • Perform animal behavior studies as needed, • Coordinate processes across departments and with outside vendors to enable efficient study execution and data generation, • Read and apply relevant scientific literature to projects to troubleshoot and solve problems, • Present research findings to project teams and prepare technical reports, • BS and/or MS in biology related field, • Extensive experience with small animal handling, • Experience with sample collection / tissue collection, • Excellent record keeping and experience in data analysis, graphing and presentation, • Ability to work independently and to handle multiple projects and deadlines, • Demonstrated innovation, creativity and resilience in problem solving, • Excellent oral and written communication skills, • Experience with CNS surgeries and/or drug administration locally in CNS, • Experiences with animal dose administration and surgical procedures, • Preclinical disease model development in the context of drug discovery California pay range $65,000—$80,000 USD Arrowhead provides competitive salaries and an excellent benefit package. All applicants must have authorization to work in the US for a company. California Applicant Privacy Policy

Job Description Job Title: Manufacturing Technician Job Description The Manufacturing Technician will be responsible for performing a range of manufacturing tasks related to reagents and buffers. The role involves troubleshooting formulations, filling processes, packaging, and conducting Quality Control procedures. You will work in a collaborative environment, supporting R&D and process improvement activities to meet production goals. Responsibilities • Perform assigned manufacturing tasks for reagents and buffers as assigned by the Supervisor/Lead., • Troubleshoot formulations, filling processes, packaging, and analytical techniques., • Conduct Quality Control procedures for consumables., • Perform data collection and analysis., • Process work orders to complete products to inventory., • Execute and improve batch records and SOPs., • Identify gaps and weaknesses in SOPs and formulations for finished goods and component materials., • Maintain accurate inventory of materials through cycle counts, ordering, and receipt of materials., • Operate in a fast-paced environment with rapidly shifting priorities., • Work as part of a multi-disciplinary team with other scientists, engineers, and manufacturing personnel., • Lead kit support and line operations., • Perform simple buffer formulation under 50L., • Provide fill support., • Experience with SOPs, BRs, and WIs., • Hands-on experience with pH, conductivity meter, UV-vis, and other standard lab equipment., • Self-motivated with the ability to work independently as well as in teams., • Highly organized and flexible., • Detail-oriented with strong analytical, verbal, and written communication skills., • Experience with developing and updating BOMs is preferred., • Experience with formulation, fill, packaging, and chromatography in a laboratory setting is preferred. The pay range for this position is $23.00 - $25.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in San Diego,CA. Application Deadline This position is anticipated to close on Oct 17, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

Job Description Beloteca, Inc. is a generic pharmaceutical development company specializing in the development of injectable products. It is desirable that the candidate have past practical experience and education in handling chemicals, operating laboratory equipment, generating and manipulating data, as well as computer database and word-processing skills. Job Description: • Independent execution of various standard laboratory techniques, including but not limited to H/UPLC, GC, water content analysis per USP, appearance assessment, water activity per USP, • May participate in qualification/verification of assays, • Assay and documentation review and report writing, • Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices., • Execution of more advanced analytical techniques with assistance such as LC/MS, DSC, and TGA, • Independent preparation of samples, solutions, instrument set-up and breakdown, • Independent preparation of data packets and creation of stability data sheets and Certificates of Analysis to summarize analytical testing, • Assisted participation in Out of Specification investigations and the documentation of analytical deviations along with Qualified Investigators and management, • BS in Biology, Chemistry and/or related science discipline., • Computer literacy in Windows applications and the MS Office., • Excellent oral and written communication skills are essential., • Minimum of 3 years experience with HPLC, UPLC, GC, Karl Fisher, pH, • Ability and willingness to work flexible hours., • Great attention to detail, quality, and a desire for success., • Self-motivated individual with the ability to learn, lead and strengthen the Beloteca, Inc. team.

Job DescriptionPosition: Business Development Manager / Director - Toxicology & Safety Assessment (Preclinical Studies) Location: Home-based - West Coast (San Diego preferred) Salary: $150,000 to $200,000 Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK, and China, we support drug discovery through to manufacturing with fully integrated, high-quality services. We're proud of the impact we make. Just last year, we supported over 1,000 preclinical safety studies, helping our clients advance their drug candidates with confidence. Our teams work across small molecules, ADCs, biologics, and gene therapies, partnering with more than 3,000 global customers. To learn more, visit . About the Role Are you a toxicologist or preclinical scientist who enjoys connecting great science with real-world impact? This could be your next step. We're looking for a scientifically minded Business Development Manager or Director to join our U.S. team, covering the West Coast, with a preference for candidates based in San Diego. This role is ideal for someone with a strong background in toxicology, safety pharmacology, or preclinical development who's ready to move beyond the bench and into a more strategic, client-facing role. You'll work closely with our internal scientists to shape proposals, ensure client expectations are realistic and achievable, and help translate complex safety assessment needs into tailored solutions. Your scientific insight will be key to building trust with clients and turning conversations into successful, long-term partnerships. It's a remote role with regular travel across the region and perfect for someone who wants to stay close to the science while stepping into a more commercial, outward-facing position. We are interviewing for this role on an ongoing basis. So don't miss out on this opportunity and apply as soon as possible. Key Responsibilities • Lead business development efforts across the West Coast, identifying and securing new opportunities with biotech and pharma clients in the toxicology and safety assessment space., • Build and maintain strong relationships with senior stakeholders, positioning Pharmaron as a trusted, long-term partner., • Collaborate with internal scientific and operational teams to develop tailored proposals and ensure successful project delivery., • Drive cross-functional initiatives to expand Pharmaron's market presence and service adoption., • Represent Pharmaron at key industry events, conferences, and client meetings., • Maintain a robust pipeline of qualified opportunities and consistently meet or exceed revenue targets., • Provide market insights and competitive intelligence to inform strategic planning.Candidate Profile, • Advanced degree in Toxicology, Pharmacology, Biology, or a related scientific discipline (PhD preferred)., • 8+ years of experience in the pharmaceutical or CRO industry, including hands-on experience in preclinical safety assessment., • Proven success in business development or client-facing roles within preclinical development., • Strong understanding of the CRO landscape and GLP-compliant safety studies., • Excellent communication, negotiation, and relationship-building skills., • Strategic thinker with a results-driven mindset and high level of self-motivation. Benefits: • Insurance including Medical, Dental & Vision with significant employer contributions, • Employer-funded Health Reimbursement Account, • Healthcare & Dependent Care Flexible Spending Accounts, • 100% Employer-paid Employee Life and AD&D Insurance, Short and Long Term Disability Insurance, • 401(k) plan with generous employer match If you have any questions about the role or application process, please contact Elisa Di Caterino - Talent Acquisition Partner on Linkedin ED1-#LI

Job Description Sanford Burnham Prebys is much more than a research facility and hub for innovation; it’s a vibrant global community of talented scientists and researchers from over 30 countries. This worldwide representation enriches our perspectives and enhances our creative approach to solving complex scientific challenges. We strive to be leaders not only in biomedical research but also in creating an environment where excellence thrives through collaboration across cultures and backgrounds. Our mission is to advance the biomedical sciences by cultivating the next generation of scientific leaders, providing meaningful opportunities for researchers of all backgrounds to learn, innovate, and make breakthrough discoveries that improve human health. Together, we translate science into health. The duties and responsibilities contained in the job description are intended to be examples of the accountabilities for which the person in the position will demonstrate competency through performance. The job description is not intended to be an all-inclusive list. Duties and responsibilities are subject to change and other duties may be assigned as necessary. Position Summary: Under direct supervision from the Breeding Colony Manager, the Lab Animal Technician II will be responsible for maintaining research laboratory mouse breeding colonies for multiple PIs/labs. Generally, the LAT II is responsible for breeding colony maintenance procedures for approximately 500-800 cages, including some cage changing. In addition, the technician may assist researchers with laboratory procedures as requested. This position involves a range of tasks and functions that are typically essential to continue critical vivarium operations. Duties and Responsibilities: All tasks are performed according to institute and industry SOPs (Standard Operating Procedures) Husbandry: • Changes cages when needed, (based on the assigned workload), per the AF Husbandry SOPs., • May perform husbandry for immunocompromised mice that require sterile caging, food, water and bedding., • May perform husbandry work in viral vector BSL-2 (Biosafety Level 2) or Quarantine animal areas., • May be assigned husbandry work in BSL-2 infectious viral or bacterial containment animal study areas., • Performs breeding colony maintenance procedures for multiple PIs., • Completes daily animal health checks; observes general health condition of each animal assigned under technician’s care. Observations include a daily check of each cage for adequate food and water, and animal health observations for pregnant animals, new litters and for signs of distress, illness, or injury due to phenotype expression or experimental procedures., • Completes and distributes health status forms to labs (e.g. sick mice, found dead)., • Breeding colony maintenance procedures include mating mice, timed mating with vaginal sperm plug check, weaning litters, ear notching mice, and collecting tail snips for genotyping purposes., • Expertise in LabTracks database management is required to maintain up-to-date and accurate breeding colony records., • Direct communication with research PI/lab contacts regarding colony maintenance requests and health findings (breeding production, non-productive breeders, sick or found dead animals)., • Updates researchers on the workflow status of their breeding colony maintenance procedure requests in a timely manner., • Reports health concerns to the Attending Veterinarian, Manager or Animal Health Coordinator and research PI/lab contact, for guidance on treatment or euthanasia., • Determines course of actions concerning animal welfare, including euthanasia, in absence of direct orders by other lab staff members, • Treats animals for routine conditions such as dermatitis or abrasions caused by aggressive behavior., • Separates aggressive animals and provides additional cage enrichment materials., • Reads the Animal Use Protocols (AUFs) to become familiar with research projects, • Notes authorized users, mouse lines and crosses associated with AUF., • Documents special care requirements for colonies under technician’s care (e.g., diets and food supplements with start and end dates)., • Maintains animal and cage census and ensures appropriate per diem rate is applied to each census record., • May perform technical procedures on animals as stated in the animal protocol (AUF), including blood collection, injection of materials (IV, IP, IM, SC), or oral dosing of drugs and compounds., • May assist Manager with cross training the LAT I staff on room and animal health checks, mating mice, timed mating/vaginal plug check, weaning litters, tail biopsy, and LabTracks database entry., • Education: High School diploma required. An Associates or Bachelor’s degree in biology or animal sciences preferred., • Experience: Two (2) years progressive lab animal experience required or equivalent education, training and/or experience from which comparable knowledge, skills and abilities have been attained, • Possess a demonstrated interest in the humane care, management, and utilization of animals in a research setting Proficiency in handling and restraint of laboratory rodents, • Knowledge of animal health, disease control/prevention, and technical procedures gained through combination of education, training and practical hands-on experience, • Knowledge of diagnosis and treatment of common laboratory rodent diseases, and identification of conditions which may result from research procedures, • Work independently as well as in a team environment, • Be responsible, organized, and a problem solver, • Possess strong attention to detail, analytical, time management, organizational, communication, and interpersonal skills, • Direct: None The vivarium is a specialized facility designed for the housing and care of laboratory animals, providing a controlled environment that ensures their health and well-being. This space is equipped with state-of-the-art housing units, environmental monitoring systems, and veterinary care areas. The vivarium maintains strict adherence to ethical guidelines and regulatory standards to promote humane treatment. The atmosphere is typically collaborative, with researchers, animal care staff, and veterinarians working closely together. Staff are required to follow established protocols for animal handling, care, and record-keeping to ensure compliance and safety. The vivarium environment is characterized by its clean and organized layout, designed for efficiency and ease of access to animal habitats. Personal protective equipment (PPE) is mandatory to maintain hygiene and minimize stress for the animals. Regular training sessions are conducted to keep staff informed about best practices in animal care, welfare, and safety procedures. Overall, the vivarium provides a dynamic work environment that emphasizes compassion, scientific integrity, and dedication to animal research. The work environment contains animal dander and dust particles. Work Schedule: • Ability to work one of the defined work schedules: 6:30-3:00 or 7:00-3:30 Monday through Friday, • Willing to work overtime if necessary to maintain integrity of a research protocol, • Ability to pass post-employment physical as required by OLAW (Office of Laboratory Animal Welfare), • Must wear institute supplied scrubs, face mask, shoe covers and hair bonnet as well as other task-related personnel protective equipment including face shield or goggles, • Working in a vivarium involves specific physical capabilities, including:, • Standing and Walking: Ability to stand for extended periods and move around the facility to attend to animal needs and maintenance., • Lifting and Carrying: Capability to lift, carry, and stack feed and bedding bags that typically weigh up to 40 pounds; and move heavy equipment (mouse housing racks and carts loaded with water bottles or caging supplies), using proper lifting, pushing or pulling techniques., • Manual Dexterity: Proficiency in handling small animals and using various tools and equipment with precision., • Repetitive Motions: Comfort with repetitive tasks involved with animal care such as feeding, cage changing and animal health checks; and animal holding room and procedure room janitorial tasks, • Bending and Stooping: Flexibility to remove and hold rodent cages from various heights within their holding rack (cages weigh 8 lbs,) for cage changing and animal health check and procedures We welcome talented individuals of all backgrounds regardless of gender, sex, religion, race, national origin, citizenship, age, disability, perceived disability, pregnancy, pregnancy-related condition, reproductive health decisions, sexual orientation, gender identity, gender expression, genetic information, HIV/AIDS, marital status, covered veteran status, or any other characteristic protected by local, state, or federal laws, rules, or regulations. We are proud to be an equal employment opportunity employer. As part of this commitment, Sanford Burnham Prebys Medical Discovery Institute will ensure that persons with disabilities are provided reasonable accommodations for the hiring process. If a reasonable accommodation is needed, please contact our Benefits Team at (858) 646-3100 or via e-mail at

Job DescriptionRincon Consultants is seeking a Director/Principal to lead our Utilities practice within the Environmental Planning and Natural/Cultural Resources teams. This is an opportunity for a proven leader in the utilities sector to shape Rincon’s statewide strategy, guide high-profile projects, and expand our market presence. You will direct multidisciplinary teams, strengthen key client relationships, and drive innovation in service delivery—while mentoring senior staff and advancing strategic growth initiatives. The ideal candidate has a strong track record in business development, complex project delivery, and regulatory navigation, with expertise in utility infrastructure, operations and maintenance planning, licensing, and energy delivery solutions. While this role may offer flexible work arrangements that can include a mix of in-office and remote work, our changing business needs will ultimately determine our level of remote-work flexibility. Additionally, to promote in-person collaboration and client teaming, we prioritize hiring those who reside within 50 miles of a Rincon office which currently includes: Carlsbad, Fresno, Los Angeles, Monterey, Oakland, Palm Springs, Riverside, Sacramento, San Luis Obispo, San Diego, San Jose, Santa Barbara, and Ventura. We are open to locations across California. Overview of Key Duties and Responsibilities Strategic Business Development and Client Leadership • Shape and lead Rincon’s statewide strategy for utilities services., • Cultivate and sustain senior-level client relationships, positioning Rincon as a trusted advisor., • Lead business development, including opportunity identification, proposal strategy, and industry representation., • Collaborate across service lines to deliver integrated solutions for transmission, distribution, power generation, and utility infrastructure projects., • Oversee project portfolios, ensuring technical excellence, compliance, and on-time, on-budget delivery., • Provide QA/QC review for technical studies, environmental documentation, and regulatory filings., • Guide strategy for CPUC, FERC, utility-specific permitting, and licensing., • Oversee planning and permitting of operations and maintenance programs, including execution of PEA (Proponent’s Environmental Assessments) and DER (Detailed Engineering Review) where applicable., • Recruit, develop, and retain top talent for the Utilities practice, fostering a high-performance, collaborative culture., • Mentor senior staff on business strategy, technical leadership, and client management., • BS or BA in Environmental Science, Biology, Ecology, Planning, or related field (MS/advanced degree preferred), • 12+ years’ senior-level experience in utilities-focused consulting, project delivery, and business development, • Demonstrated ability to lead complex, multidisciplinary projects, navigate regulatory frameworks, and deliver strategic solutions for clients, • Experience in licensing, permitting, and programmatic compliance for utility infrastructure projects, • Knowledge of CPUC processes, General Orders, and utility O&M permitting, • Proven track record of building long-term client relationships and securing repeat business, • Strong business acumen with expertise in budgeting, forecasting, and resource allocation, • Exceptional communication and presentation skills The base salary range for this full-time position is $140,000–$190,000+, plus a generous benefits program. At Rincon, our salary ranges are based on market median of similar jobs, according to third party salary benchmark surveys. The base pay that is offered will consider internal equity and may vary depending on the candidate’s job-related knowledge, skills, and experience. We are proud to offer a comprehensive Total Rewards Package, providing our valued employees with many benefits to enhance their well-being and financial security. Our health benefits include a range of options such as HMO, PPO, HDHP, and Health Savings Account choices, ensuring you have the flexibility to select the plan that best suits your needs. Additionally, you can enjoy peace of mind with employer-paid life and long-term disability insurance, as well as dental, vision, and prescription drug coverage. We prioritize your well-being by offering three weeks of vacation accrual in the first year, paid sick leave, and paid holidays, ensuring you have ample time off to rejuvenate. Planning for your future is made easier through our 401(k) / Profit Sharing Retirement Plan and bonus opportunities. Beyond the essentials, Rincon recognizes the importance of personal and professional growth, that's why we provide opportunities for professional development and mentoring. Our commitment extends to the community through Volunteer Pay for a Day, reinforcing the values of social responsibility. Moreover, we go the extra mile with additional perks like Flexible Spending & Dependent Care, Supplemental life insurance, Legal Shield, Identity Protection, Pet Insurance, and much more. Check out more details on our Rincon Consultants webpage here! Individuals offered employment must successfully complete a pre-employment drug screening as a condition of employment. Additionally, those hired who may be assigned to federal projects will be subject to further drug testing, including screening for cannabinoids (THC/marijuana), in compliance with the Drug-Free Workplace Act of 1988 and other applicable federal regulations. Rincon Consultants, Inc does not accept unsolicited applicant/candidate resumes from search firm recruiters and/or temporary agencies that do not have a signed contract and specified work order with Rincon Consultants. Further, such resumes received will be deemed the sole property of Rincon Consultants and no fees will be paid in the event Rincon Consultants subsequently hires such individual. Rincon Consultants is an equal opportunity employer. All aspects of employment will be based on merit, competence, performance, and business needs. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. Powered by JazzHR KAJhDjqcj2

Key Requirements and Duties: The Clinical Laboratory Scientist I (CLS I) will perform analytical testing as well as general laboratory processes, in a high complexity clinical molecular laboratory in compliance with policies, procedures and regulations. Responsibilities: • Performs clinical testing of patient samples, which includes set-up of molecular assays., • Adheres to the laboratory’s quality control processes and document quality control activities, instrument and equipment verifications, and instrument maintenance and preventive maintenance., • Supports the Corporate and Laboratory Operations Goals and Objectives., • Follows the laboratory's policies and procedures whenever test systems are not within the laboratory's established performance specifications., • Identifies and documents problems that may adversely affect test performance and notifies the manager or director., • Documents all corrective actions taken when test systems deviate from the laboratory's established performance specifications., • Participates in activities required to support all necessary licensure for the clinical laboratory, including maintaining quality systems and test records and supporting on-site inspections of the laboratory., • Utilizes an in-house Lab Information System (LIS)., • Complies with all local, state, and federal laws and regulations governing clinical laboratory operations., • Maintains records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens., • May be required to monitor the activities of non-licensed personnel., • May be required to assist in assay development activities., • Performs other duties as assigned. Minimum Education/Experience Requirements: • Clinical Genetics Molecular Biologist (CGMBS) or Generalist Clinical Laboratory Scientist (CLS) License from the State of California, • Bachelor’s Degree in Medical Technology or Biological Sciences., • Must meet the requirements for Testing Personnel under CLIA 88 (42 CFR, part 493), • Highly organized, able to work independently, follow standard operating procedures., • Experience in a high complexity CLIA/CAP environment strongly preferred, • Experience in Molecular Biology, Molecular Pathology, and/or Medical Genetics preferred Required Training/Certification: • On the job training including, but not limited to: HIPAA, and safety procedures.

Job Summary Bancroft Construction Services specializes in delivering environmentally responsible construction solutions that balance infrastructure development with ecological protection. We are seeking a Qualified SWPPP Developer (QSD) to support our environmental compliance team in ensuring stormwater pollution prevention measures are implemented effectively on active construction sites. As a QSD, you will be responsible for developing, implementing, and monitoring Stormwater Pollution Prevention Plans (SWPPPs) to ensure compliance with state and federal regulations. You’ll play a critical role in supporting construction teams, protecting sensitive resources, and maintaining project timelines while meeting regulatory requirements. Location: Remote 50-75%, site visits 25-50% in the Southern California Region. Key Responsibilities • Develop, update, and certify SWPPPs in compliance with state and federal stormwater regulations., • Conduct site evaluations and risk assessments to determine appropriate Best Management Practices (BMPs)., • Oversee implementation of stormwater management measures on active construction sites., • Perform routine site inspections, audits, and water quality sampling as required., • Train field staff on stormwater compliance and BMP installation/maintenance., • Collaborate with project managers, superintendents, and environmental staff to ensure compliance throughout all phases of construction., • Prepare inspection reports, compliance documentation, and regulatory submittals., • Track corrective actions and provide recommendations for adaptive management. Qualifications • Current QSD certification (required)., • Bachelor’s degree in Environmental Science, Civil Engineering, Biology, or a related field preferred., • 3+ years of experience in stormwater compliance, construction site inspections, or environmental management., • MS4 permit consulting experience, • Strong knowledge of federal, state, and local stormwater regulations (e.g., CGP, NPDES, CWA)., • Excellent communication and report-writing skills., • Ability to work independently in the field and collaborate with diverse project teams., • Willingness to travel to job sites as needed Pay: Starting salary of $85,000/annually Benefits: • Competitive compensation based on experience and skills., • Training provided., • Opportunity to work with a dynamic and diverse team., • Potential for growth based on performance., • Excellent benefits program. About Bancroft: Our mission at Bancroft Construction Services is to provide quality environmental compliance consulting services with honesty, sincerity, and diligence. By providing environmental compliance consulting services, we demonstrate our devotion to ensuring California’s waterways remain pure and unpolluted and its precious biological and cultural resources are protected and preserved for generations to come. We have a successful history working on a wide variety of projects, from California High Speed Rail Construction Package 4 to the Skookumchuck Wind Energy Project. We also have experience working on high-profile projects with companies such as Southern California Edison. Bancroft Construction Services, LLC is an Equal Opportunity Employer that does not discriminate on the basis of actual or perceived race, color, religious creed, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth and related medical conditions), gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, protected medical condition as defined by applicable state or local law (such as cancer), genetic information, or any other characteristic protected by applicable federal, state or local laws and ordinances. Bancroft Construction Services, LLC’s management team is dedicated to this policy with respect to recruitment, hiring, placement, promotion, transfer, training, compensation, benefits, employee activities, access to facilities and programs and general treatment during employment.

Bio-Studies is a growing natural resources consulting firm in Southern California providing quality natural resources consulting services to a diversity of clientele. Our team of biologists offer natural resource management services, including wildlife and botanical surveys, construction monitoring, desktop analysis, GIS mapping, regulatory expertise, project management, and regulatory permitting. Bio-Studies provides opportunities for work in Southern California and across the Southwest United States. Our Mission: Our Mission is to provide comprehensive, innovative, and project-specific solutions to the complex scientific and regulatory issues facing our local environment. We are committed to providing positive, science-based outcomes for our clients. Available Positions: We are seeking botany and wildlife biologists with varying levels of experience to support natural resource and construction projects. We are currently hiring for: • Project Biologists. The project will require the ability to work independently and monitor compliance with natural resource management for projects. The ideal candidate will have 2-5 years of experience with relevant experience either in the region or similar type of projects. Candidates will require relevant field experience and suitable for early-career biologists looking to develop their skill set! Is this role for you? • The ideal candidate will be organized, motivated, flexible, and able to support projects throughout Southern California and Arizona., • Candidates are available to work full-time, with some over-time., • This role is project and location based initial project is likely one year commitment with possible travel up to 14 days a month. Duties may include botanical, wildlife, or wetland field surveys and construction monitoring in a variety of terrains and weather conditions. Familiarity with an array of data collection techniques, including ESRI software applications, is preferred. Facility with data entry and report writing will be required. Biologists will work independently but be supported by the Bio-Studies Project Managers and Senior Staff. Correspondence and coordination with clients, other Bio-Studies employees and construction contacts will be required. Resilient and motivated candidates will note that the role at times requires extended work hours, long field days, often requiring remote travel, and overnight stays up to 2 weeks may be required depending on the project. All biologists will direct report to Senior Staff, but are required to independently monitor reporting responsibilities, record their timesheets, submit timely expense reports, and provide daily field reports. Staff will be provided with mentorship in their role but are expected to be initiative-taking to develop their skill set in terms of technical writing and field survey techniques. Bio-Studies can provide a flexible work environment; work schedules may fluctuate based on project construction or seasonal timelines. Duties include: • Biological survey fieldwork for wildlife and botanical resources and habitat, including endangered species, conducted alone, or as part of a team., • Environmental compliance monitoring, including coordinating with others; conducting worker environmental awareness programs, working on-site with construction crews, and performing post-construction analysis., • Utilizing electronic data collection methods and managing data, including writing daily technical reports, preparation of technical studies and full reports., • Working remotely, being self-sufficient, trustworthy, and upholding company standards conducting work in a safe manner pursuant to the Company’s Safety Policy, promptly and accurately billing time to assigned work projects, and complying with all Company and client policies., • Maintaining work calendars, regularly communicating changes in availability with advance notice., • Maintaining a professional, punctual, and enthusiastic attitude with colleagues and clients and clear and concise communication., • Ability to adapt in a dynamic and challenging work environment., • Performing work and meeting deliverables during working hours; submits all deliverables, reports, or requested changes within specified deadlines., • Ability to meet the physical demands required for fieldwork, with reasonable accommodations., • Safe operation all Company provided, or personal vehicles used for Company purposes and pursuant to the Company’s Vehicle Policy. Qualifications: • Bachelor’s Degree or higher in biology, ecology or related field and 6 months+ of experience in biological field work, • Self-motivated, takes initiative, and able to work remotely with remote supervision for months at a time., • Confident time management and follow-through skills, ability manage multiple tasks/projects and stick to deadlines., • Technologically proficient with handheld electronic devices and proficient in computer software including MS Outlook, Word, Excel, and Teams., • Must carry valid Driver’s License with vehicle insurance for personal vehicles used for Company purposes or be insurable under Company’s liability insurance policy for use of Company Vehicles., • Off-road and 4x4 driving experience preferred., • Must obtain clearance through client’s federal background check, • Must adhere to and support Bio-Studies’ commitment to diversity, equality, and inclusion. Working Conditions: Project work occurs in diverse outdoor environments and can include hiking over rugged terrain and long distances, inclement weather, and driving into remote areas, on and off road. Most projects require long distance travel in a variety of field conditions for multiple weeks at a time and hotel lodging is offered. Safety risks that may be encountered on the job include dangerous wildlife (e.g., ticks, bees, rattlesnakes, scorpions, mountain lions), wary or hostile public, challenging driving conditions, construction site hazards, and extreme weather conditions (heat, cold, rain, wind). Bio-Studies provides a Company Safety Plan as well as required safety trainings. Compensation: Project Biologist - $25 - $35 per hour depending on need, skills, and experience. Benefits may include: Health Insurance (Medical, Dental, and Vision)*, 401k, cell phone and/or other digital devices, paid training opportunities, and remote work and travel opportunities. *Eligibility is dependent on duration of work and workload (hours per week). To Apply: Interested applicants should submit a resume and brief cover letter detailing your interest, qualifications, a sample of your technical writing, three references, and any special considerations or compensation expectations. All submissions should go to . Resumes received without a cover letter or references will not be considered. EEO Statement: We believe in hiring employees based on their qualifications and skills. We do not discriminate against any protected class including, but not limited to, race, color, ancestry, national origin, religion, creed, age, disability (mental or physical), sex, gender, sexual orientation, gender identity, gender expression, medical condition, genetic information, marital status, military, or veteran status.

About the Role The client is an innovative early-stage biotech organization focused on accelerating drug development and advancing personalized medicine through multi-omics solutions. Leveraging cutting-edge mass spectrometry technology, advanced computational tools, and comprehensive human health data, the client enables rapid biomarker discovery at scale. This approach provides deeper insights into human biology and aligns therapeutic targets with patient populations to improve treatment precision and outcomes. The team consists of highly collaborative scientists, clinicians, and engineers committed to scientific rigor and transformative innovation. Position Overview We are seeking a dynamic Proteomics Principal Investigator to lead complex proteomics initiatives, foster scientific breakthroughs, and strengthen client partnerships. This role requires deep expertise in mass spectrometry-based proteomics, strong leadership capabilities, and proficiency in integrating multi-omics data to deliver actionable insights within a regulated CRO setting. The ideal candidate excels in collaborative environments, mentors high-performing teams, and sets the standard for scientific excellence. Key Responsibilities • Partner with leading experts to promote growth through advanced training and knowledge-sharing., • Oversee project execution between the client and internal wet- and dry-lab teams, ensuring timely delivery and resolving challenges as needed., • Design research strategies, develop study plans, and prepare comprehensive reports., • Analyze mass spectrometry data, review spectra, and identify compounds., • Guarantee data integrity and compliance with quality and regulatory standards., • Compile findings into presentations and deliverables for stakeholders., • Manage multiple projects simultaneously, ensuring timelines and objectives are met., • Interpret complex scientific results and stay current with emerging technologies and literature. Required Experience • Minimum 5 years in CRO, pharmaceutical, or biotech environments with hands-on experience in LC-MS/MS platforms (Orbitrap, Q-TOF, timsTOF) and data analysis workflows (DDA, DIA, PRM, MRM/SRM, TMT/iTRAQ, PTM)., • At least 5 years in a leadership role managing scientific teams and projects., • Demonstrated ability to design and execute advanced proteomics experiments (discovery, targeted, PTM analysis)., • Proven track record in client-facing roles, scientific presentations, and cross-functional collaboration. Qualifications • PhD/MD in a relevant discipline (chemistry, biochemistry, biology, pharmacology, or related life sciences) or equivalent experience. BS + 10 years or MS + 5 years relevant experience., • Strong background in mass spectrometry-based proteomics and data interpretation., • Experience with metabolomics and proteomics methodologies., • Skilled in managing multiple priorities, mentoring teams, and delivering results under tight timelines., • Ability to communicate complex scientific concepts clearly in both written and verbal formats., • Collaborative mindset with experience working alongside multidisciplinary teams., • Detail-oriented with a commitment to accuracy and reliability., • Up-to-date knowledge of precision medicine advancements. Role Impact This is a client-facing leadership position, serving as a strategic partner to laboratory operations. The role involves managing 15+ client programs, contributing to study design, developing project plans, and ensuring seamless communication between clients and internal teams to deliver transformative biological insights across diverse therapeutic areas.

The Clinical Laboratory Scientist I (CLS I) will perform analytical testing as well as general laboratory processes, in a high complexity clinical molecular laboratory in compliance with policies, procedures and regulations. Responsibilities: • Performs clinical testing of patient samples, which includes set-up of molecular assays., • Adheres to the laboratory’s quality control processes and document quality control activities, instrument and equipment verifications, and instrument maintenance and preventive maintenance., • Supports the Corporate and Laboratory Operations Goals and Objectives., • Follows the laboratory's policies and procedures whenever test systems are not within the laboratory's established performance specifications., • Identifies and documents problems that may adversely affect test performance and notifies the manager or director., • Documents all corrective actions taken when test systems deviate from the laboratory's established performance specifications., • Participates in activities required to support all necessary licensure for the clinical laboratory, including maintaining quality systems and test records and supporting on-site inspections of the laboratory., • Utilizes an in-house Lab Information System (LIS)., • Complies with all local, state, and federal laws and regulations governing clinical laboratory operations., • Maintains records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens., • May be required to monitor the activities of non-licensed personnel., • May be required to assist in assay development activities., • Performs other duties as assigned. Minimum Education/Experience Requirements: • Clinical Genetics Molecular Biologist (CGMBS) or Generalist Clinical Laboratory Scientist (CLS) License from the State of California, • Bachelor’s Degree in Medical Technology or Biological Sciences., • Must meet the requirements for Testing Personnel under CLIA 88 (42 CFR, part 493), • Highly organized, able to work independently, follow standard operating procedures., • Experience in a high complexity CLIA/CAP environment strongly preferred, • Experience in Molecular Biology, Molecular Pathology, and/or Medical Genetics preferred, • The candidate must have a Clinical Genetic Molecular Biologist Scientist (CGMBS) or Generalist Clinical Laboratory Scientist License by the State of California. Manager Notes: Technology Requirements: The preferred candidate should have experience with manual and automative pipetting of patient samples and reagents. The preferred candidate should have real-time PCR experience. The candidate should have experience manually pipetting reagents accurately to create master mixes for the assay. What does a typical day look like? (daily tasks) The candidate will process oncology samples starting with RNA extraction, reverse transcriptase, pre-amplification, and real time PCR in a molecular clinical laboratory. Preferred background/prior work experience? The preferred candidate should have experience with molecular biology or oncology in a CLIA laboratory. Experience with Tecan instruments in a plus. Training/Certification: • On the job training including, but not limited to: HIPAA, and safety procedures. Priority soft skills 1. Strong attention to detail, 2. Strong communication skills, 3. Strong teamwork and ability to collaborate, 4. Strong time management skills, 5. Strong Ethical Judgment & Integrity

At HAYA Therapeutics, we are revolutionizing RNA-guided genome-targeting therapies to treat fibrosis, heart failure, and other serious diseases associated with aging. Our innovative platform leverages long non-coding RNAs (lncRNAs)—key regulators within the “dark matter” of the genome—to develop first-in-class, highly specific therapies that modulate gene expression and restore cellular function. Recognized for our innovation, HAYA received the prestigious Innosuisse Certificate for Sustainable Growth and has been nominated as TOP Innovative Companies in Switzerland 2025. HAYA's vision is to pioneer the development of next-generation biopharma, leveraging causal disease biology and AI-enabled functional genomics and systems biology to develop precision disease-modifying therapies for common and chronic diseases. By unlocking the full potential of the regulatory genome, our platform enables rapid de-risked target discovery and scalable drug development across multiple therapeutic areas. As a fast-growing biotech, we offer an entrepreneurial, science-driven environment where you’ll have a direct impact on shaping our pipeline and advancing RNA medicine. Position Summary: HAYA Therapeutics is seeking a talented and experienced Computational Biologist with deep knowledge of cardiac biology and transcriptomics to join our data science team. In this highly collaborative and impactful role, you will leverage bulk, single-cell and single-nuclei transcriptomic and epigenomic omics data to drive translational research and biomarker discovery in cardiac settings. You will apply innovative computational approaches to uncover novel biology and therapeutic opportunities relevant to cardiac diseases. HAYA deploys a combination of experimental and computational solutions for target and drug discovery in the non-coding regulatory genome space. To this end, we leverage multiple omics modalities, including transcriptomic profiling (e.g., single-cell and single-nuclei RNA-Seq, bulk RNA-Seq). You will apply your end-to-end expertise in transcriptomics data preprocessing and downstream analysis to contribute to scientific discoveries and the advancement of our precision RNA-based therapeutics for cardiovascular diseases. The entire Data Science team across Haya programs will use the analysis templates and approaches you establish to handle complex datasets. The Data Science team is central to HAYA’s vision by pioneering innovative AI and advanced computational biology solutions to overcome current scientific, methodological, and operational bottlenecks. We leverage complex biological datasets to remove operator biases, enabling the rapid end-to-end execution of HAYA’s pipeline. Our approach ensures precision-driven decision-making, which enables target drug discovery, biomarkers, translational, clinical, and business strategies, reinforcing HAYA as a leader of next-generation biopharma. What’s in it for me? At HAYA, you won’t just analyze data - you’ll help shape the future of RNA-based therapeutics. This is a unique opportunity to apply your scientific expertise to uncover novel biology in the non-coding regulatory genome and translate those discoveries into real therapeutic potential. You’ll be part of a deeply collaborative and forward-thinking team, working at the intersection of data science, functional genomics, and drug discovery. Here, your insights won’t sit on a shelf - they’ll directly influence the development of treatments for patients with serious cardiovascular and fibrotic diseases. We offer a dynamic, innovative culture where scientific curiosity is celebrated, your voice is heard, and your growth is supported. Whether you're leading high-impact projects, engaging with cross-functional teams, or learning something new every day, you’ll find a meaningful and rewarding career path at HAYA. Key Responsibilities: • Perform bulk, single-cell, and single-nuclei transcriptomics computational analysis, mainly on (but not limited to) cardiac tissue and disease-related data., • Be an internal expert on cardiac transcriptomics, consulted across multiple settings including target MoA and validation, biomarkers, translation, and pre-clinical and clinical settings., • Conduct in-depth investigations using both in-house and publicly available datasets to uncover cardiac disease- and perturbation-specific cell states and transcriptional programs., • Integrate transcriptomic data (including single-cell data and bulk RNA-Seq) from multiple independent datasets to inform biomarker discovery and validation strategies., • Prepare and communicate high-quality scientific reports, visualizations, and presentations for both technical and cross-functional stakeholders. Education & Experience: • PhD in computational sciences (e.g., bioinformatics, computer science) or life sciences with a strong computational focus, or equivalent industry experience (6+ years)., • Deep expertise in transcriptomic data analysis, including single-cell and single-nuclei RNA-Seq and bulk RNA-Seq data analysis, covering preprocessing, integration, and biological interpretation., • Deep knowledge on cardiac biology and cardiac diseases, including HCM and HF, and ability to relate it to transcriptional dynamics across different cell types and states., • Proven ability to integrate data from multiple sources to construct clear, biologically meaningful narratives, with a demonstrated track record of delivering high-quality single-cell/nuclei RNA-Seq and bulk RNA-Seq data packages., • Proficient in R or Python, with experience working in Linux-based computing environments, including remote server access and basic Bash scripting., • Experience with primary epigenomic data analysis (e.g., ATAC-Seq, PRO-Seq, GRO-Seq, CUT&RUN, chromatin conformation capture) to identify functional regions in the regulatory genome is a plus., • Excellent written and verbal communication skills in English, with the ability to clearly present complex data to diverse audiences. HAYA Therapeutics is an Equal Opportunity Employer committed to fostering a diverse, inclusive, and equitable workplace where all individuals feel valued and empowered. We provide equal employment opportunities to all qualified applicants and employees without regard to race, color, religion, sex (including pregnancy, sexual orientation, gender identity, or gender expression), national origin, ancestry, age, marital or familial status, veteran status, disability, genetic information, or any other characteristic protected by applicable federal, state, or local laws. We prohibit discrimination and harassment of any kind and are committed to ensuring fair and equitable treatment in all aspects of recruitment, hiring, promotion, compensation, benefits, training, and career development. At HAYA, we believe that diversity of thought, experience, and background drives innovation and strengthens our mission to transform patient care through cutting-edge RNA-based therapeutics.