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Job Description Heartland Food Products Group is a global leader in the consumer packaged goods (CPG) industry, producing low-calorie sweeteners, coffee, coffee creamers and liquid water enhancers. We manufacture and market Splenda, the #1 brand in the low calorie sweetener category and the most recognized in the world. We make coffee, tea and water taste better and help people live happier, healthier and longer lives by making it easy to reduce sugar. We offer an excellent compensation and benefits package. Come grow with us! This role is not a remote opportunity, it is on-site at our Manufacturing Plant in Indianapolis, Indiana. Scope: The Sanitation & Validation Manager is responsible for managing several key prerequisite programs including – calibration of equipment, validations of preventive controls, and performance metrics measuring effectiveness of sanitation activities. These sanitation activities encompass – master sanitation, environmental monitoring and operator CILs. This individual works in conjunction with the Food Safety & Quality Assurance Manager developing policies and standards to ensure the plant is prepared for any inspection. They work across the organization to educate and drive adherence to policies and standards. Essential Duties and Key Responsibilities: • Develop and implement prerequisite programs to drive food safety around plant hygiene., • Enhance and maintain a Master Sanitation Schedule and operator Clean, Inspect, Lubricate (CILs) activities., • Work with the sanitation team and plant managers to ensure adherence to the MSS., • Lead CIP validation studies and evaluate results., • Partner with engineering to drive hygienic design., • Review, update, and develop SSOPs., • Manages the execution of the Environmental Monitoring Program and results., • Conduct investigations and perform RCA/CAPAs when out of Specification results occur., • Establish strong relationships throughout the organization. Ability to work in a collaborative environment., • Reviews calibrations of equipment and ensures appropriate actions are taken to address nonconformances., • Participates in development and execution of validation protocols for preventive controls which are scientific and thorough., • Maintains a work environment committed to sustainable safety by enforcing safety rules, setting a safe example, and coaching and communicating to associates the reasons for safe operations., • Participate in internal audits and external audits, including annual SQF recertification audit., • Communicate clearly and effectively, both orally and in writing, at all levels of the organization., • Differentiate among competing demands and establish or shift priorities as needed., • Organize and coordinate multiple tasks and to work under time pressure to meet deadlines., • Ability to multi-task and work within aggressive timeframes with minimal supervision., • Experience with HACCP Plans and an understanding of dairy / food microbiological principles., • Familiarity with microbial flora and fauna found in food (dairy) plants and monitoring and control programs associated with these., • Experience with regulatory and third party audits (e.g. SQF, BRC, FSSC 22000), • Bachelor's degree in Biology, Microbiology, and / or Food Science a minimum. Demonstrated experience with food or nutritional products manufacturing and / or quality programs required. Familiarity with food / nutritional product legislation (FDA & USDA 21CFR & 9 CFR) a plus., • HACCP, PCQI Certification, • Familiar with current good manufacturing requirements, • Good analytical and problem-solving skills; good attention to detail and ability to follow written and oral instructions., • Must work well in a team environment and have strong communication skills, • Must have the ability to perform under pressure and communicate well with all departments, • Must have good computer skills, including proficiency with MS Office, MS Project, MS Excel, Basic, • Must be able to physically perform the functions of climbing, balancing, stooping, kneeling, crouching, reaching, standing, walking, pushing, pulling, lifting, grasping, feeling, talking, hearing, and repetitive motions., • Must be available to work during extended or off-hours, • Must be able to work seated using a computer and phone for long periods of time., • Must possess visual acuity to document company records., • Continuous walking throughout plant and distribution center., • Lifting up to 40 pounds #IND2

Job DescriptionHIRING NOW: Quality Control/Assurance Laboratory Tech INTERVIEWS AVAILABLE THIS WEEK Interested in this role? Reach out directly to grawilliams@actalentservices .com or CALL / TEXT: 317 567 6610 with an updated resume to apply(HIRING NOW) Position Summary The Quality Assurance Technician plays a vital role in ensuring compliance with food safety and quality standards by testing finished products, packaging, and raw materials. This role is also responsible for supporting internal audits, maintaining lab equipment, and cross-training within chemistry labs. Key Responsibilities • Test finished goods, raw materials (milk, oil, corn syrup), and packaging for compliance., • Conduct cream release and component testing; perform identity (ID) testing of raw materials., • Calibrate Charm SL equipment and prepare FT2 cleaning/zero solutions., • Maintain clean, organized, and compliant laboratory conditions., • Monitor and document refrigeration and incubator temperatures., • Manage inventory and ordering of lab consumables., • Record and review test data using GDPs and GLPs., • Execute Internal Control Plan and enter data in SAP and other systems., • Trend lab data and report findings to operations., • Promptly escalate any out-of-spec results., • Perform routine quality and food safety audits., • Contribute to continuous improvement initiatives., • Bachelor’s degree in a life science field (e.g., Biology, Chemistry, Food Science)., • Laboratory experience, including that acquired through education., • Understanding of GMP, HACCP, SQF, and food safety regulations., • Familiarity with wet chemistry, titration, and chemical testing., • Third-shift lab environment with a small team (2 others)., • Time split between lab and production floor to conduct sampling and testing., • Initial training on first shift (Mon–Fri, 8 AM–5 PM). • I am scheduling interviews for this position and conducting phone interviews as early as today. All candidates will be considered immediately within 24 hours of applying directly to Grace Williams. 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 Indianapolis,IN. Application Deadline This position is anticipated to close on Oct 15, 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 Environmental Staff Scientist Job Responsibilities The Environmental Staff Scientist will assist in the implementation of turn-key groundwater and soil remediation designs utilizing our custom designed injection trailers equipped with specialized tanks, pumps, hoses, flow meters, pressure gauges, and injection tooling at project sites around the United States. Additional responsibilities include, but are not limited to, the following: · Support on-site management for implementing Scope of Work (SOW) • review and understand site specific remediation SOW, • assist with product handling, mixing, and preparation, • record locations of application points, injected volumes, and general field observations Pay/Benefits: This position will be within the range of $24.00/hour - $26.00/hour, plus overtime. REGENESIS offers a generous benefits program including paid time off (PTO), life insurance, health insurance for employees and their families and employees a 401K program.

Job DescriptionCompany Description The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. 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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you’re looking for a rewarding career, a place to call home, apply with us today! Job Description Responsibilities include but are not limited to: • Perform cell-based bioassays and surrogate bioassays such as ligand-binding ELISA assays in plate-based format in a GMP environment, • Perform qualification and transfer of analytical test methods in the GMP environment, • Document laboratory work in notebooks/electronic notebooks and log books, perform data integrity checks, data verification reviews, and communicate final results through electronic systemsQualifications, • Bachelor’s degree in life science concentration (chemistry, biology, or related fields) and 2 to 4 years of directly related industry experience or a MS degree in a life science concentration (chemistry, biology, or related fields) and a minimum of 2 years of directly related industry experience., • Authorization to work in the United States indefinitely without restriction or sponsorship, • Strong computer, scientific, and organizational skills, • Experience with reporter-gene assay, cell biology skills such as cell culturing, cell counting, cell banking; GMP quality system and lab operations experience, • Excellent communication (oral and written) and attention to detail, • Ability to work independently and as part of a team with internal and external clients, self‑motivation, adaptability, and a positive attitude, • Ability to learn new techniques, keep accurate records, follow instructions, and comply with company policies Additional Information • Position is full-time, Monday-Friday, 8:00 am - 5:00 pm., • Base pay range: $22.96 - $25.13 per hour, based on degree and relevant experience level., • Candidates currently living within a commutable distance of Indianapolis, IN are encouraged to apply, • 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, • #LI-EB1 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job DescriptionSalary: Senior Scientist - Gene-to-Structure Helix BioStructures, LLC (HBS) is a contract research organization based in Indianapolis, Indiana, providing early drug discovery services to the biopharmaceutical industry. HBS maintains a full suite of services that encompass chemical & structural analysis, protein production, computational modeling, and design. HBSs core and most popular services are structural biology imaging techniques: X-ray Crystallography and Cryo-EM. HBS was founded in 2018 and has grown considerably. We are looking to add an experienced senior scientist to join our Indianapolis-based team. Main Responsibilities This senior-level scientist will support our protein production and structural biology pipelines by producing proteins and setting up crystallization and/or cryo-EM experiments, interfacing with our clients, and writing technical project reports. The scientist will be expected to improve upon current state-of-the-art methods to accelerate research processes. This scientist will also be responsible for managing and supporting the team, planning & tracking all projects to produce and deliver high-quality work to our clients. A proven track record in managing people and projects with a deep understanding of protein construct design, expression, and purification of challenging proteins, biophysical characterization, and structural biology techniques is essential. Highly desirable hands-on experiences include: (a) Broad experience in protein production, both expression and purification (mammalian and prokaryotic) (b) Biochemical, biophysical, and structural characterization of over-expressed and purified proteins. (c) Crystallizing proteins and nucleic acids. (d) Cryo-EM grid preparation, data collection, and processing. (e) Structure building and refinement program usage to phase difficult data sets. In addition to expertise in crystallography and/or cryo-EM, this scientist will employ a range of experimental strategies (biochemical, biophysical, and/or computational) to support our clients structure-based drug discovery, antibody discovery, and/or protein engineering. Accordingly, proficiency and a passion for exploring the structural basis of protein-protein and protein-ligand interactions are essential. The successful candidate will be a technical expert who can lead from the bench and collaborate with colleagues on multiple projects in parallel. Overall, you will be an outstanding protein scientist and structural biologist, collaborator, project and people leader who will significantly impact our portfolio with the unique opportunity to help drive discovery projects from inception to early development. Additional Responsibilities • Document experimental data and communicate research priorities, progress, and results with clients/project teams., • Provide the team with project details, priorities, technical and scientific guidance, deliverables, and timelines., • The candidate will be responsible for managing the team and all projects and providing support for project success., • This candidate will manage his/her direct reports and provide all the support they need., • The candidate will be responsible for timely updates on project statuses, reporting to their supervisor informally and to Helixs customers by formal report writing and oral presentations. Required Qualifications • Ph.D. in biochemistry, biophysics, protein engineering, and/or structural biology with experience on multiple challenging protein targets. Productive postdoctoral training and/or industry experience is expected., • Industry experience: 3-7 years post-Ph.D. (not including time as an academic postdoc)., • Demonstrated competency in protein expression and purification strategies using bacterial, insect, and/or mammalian cell lines., • Demonstrated knowledge of construct design for structural/biophysical studies and biophysical characterization of proteins., • Extensive experience in protein X-ray crystallography from protein sample assessment, crystallization, optimization, and data collection to structure determination and refinement., • Experience with model building and refinement software, such as Phenix, Autoproc, CCP4, Chimera, Rosetta, ShelX, Coot, and Pymol., • Experience with crystallization robots and standard analytical techniques associated with assessing protein quality during purification., • Extensive experience reproducing and advanced optimization of crystal hits to produce diffraction-quality crystals., • Extensive experience with co-crystallization and soaking techniques to help produce ligand-bound protein structures., • Demonstrated experience and knowledge in people and project management., • Strong leadership, written and oral communication skills, and attention to detail. Additional qualifications • Hands-on experience engineering protein constructs and optimizing the production of protein targets for structural and functional studies., • Experience in biophysical characterization tools and strategies., • Ability to generate and characterize milligram quantities of high-quality protein reagents, • Experience with protein engineering and/or design approaches., • Analysis, design, and/or computational approaches to investigate ligand-protein complexes., • Experience with Cryo-EM is a plus, especially grid vitrification, screening, and data processing using RELION., • Lead and provide technical and scientific guidance to the team and manage all projects to produce high-quality results and meet the timeline., • Excellent communication, interpersonal, organizational, and management skills., • Fearless attitude to tackle longstanding complex problems. Location This position is based in Indianapolis, Indiana, and does NOT offer a hybrid option. Interaction with external service vendors is also expected. Physical Requirements Able to lift 30 lb objects. Able to visualize microscopic objects under microscopes. Non-standard work schedule, travel, and lab safety Able to adhere to safe work practices and perform lab work with appropriate personal protective equipment such as but not limited to safety goggles, facial mask, gloves, lab coat/ protective gowning, and closed-toe shoes. Able to work at flexible hours occasionally when performing time-sensitive experiments. Other job details • Eligible for Relocation Assistance, • Competitive Salary + Bonus, • Competitive PTO, • Retirement (matching 401K), • Health/Dental/Vision Insurance, • Company Apple computer Helix BioStructures, LLC is an equal opportunity employer, and we embrace the increasingly diverse world around us. Helix BioStructures, LLC prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin or ancestry, age, disability, marital status, and veteran status.

Job DescriptionHeartland Food Products Group is a global leader in the consumer packaged goods (CPG) industry, producing low-calorie sweeteners, coffee, coffee creamers and liquid water enhancers. We manufacture and market Splenda, the #1 brand in the low calorie sweetener category and the most recognized in the world. We make coffee, tea and water taste better and help people live happier, healthier and longer lives by making it easy to reduce sugar. We offer an excellent compensation and benefits package. Come grow with us! This role is not a remote opportunity, it is on-site at our Manufacturing Plant in Indianapolis, Indiana. Scope: The Compliance Manager plans, directs, and coordinates all activities in accordance with current regulation and policy. Their responsibilities include the management of specifications, review of labels and claims, net contents, and supplier performance of both packaging and raw materials. This position is required to consult and provide expertise to company personnel regarding compliance and regulatory requirements. Essential Duties and Key Responsibilities: • Maintains a work environment committed to sustainable safety by enforcing safety rules, setting a safe example, and coaching and communicating to associates the reasons for safe operations., • Manages material sampling and monitoring programs to ensure the safety and compliance of materials by identifying and minimizing risks and managing contaminants., • Manages specification creation (MPSEC) and label declarations processes. This includes all Quality activities related to artwork creation, maintenance, and revisions., • Manages the receiving and Ingredient and Finished Product COA process., • Responsible for Supplier Quality pre-requisite program:, • Vendor Approval,, • Approval of RAW/PACKs,, • Vendor Performance Management and Review, aligned with Procurement. Supplier SCAR management, investigation and reporting., • Drives compliance with regulations foreign and domestic by preparing the organization with information about consumer and industry trends, emerging threats, and evolving laws and regulations. This includes establishing systems to ensure compliance with all legal requirements., • Management of Databases and Team Rooms for these processes., • Act as back up for Verification and Audit Manager, • Serve as alternate SQF practitioner, responsible and authorized for ensuring company fulfills all requirements of the current SQF code, • Responsible for driving compliance and maintenance of all certifications – including GFSI, cGMP, Kosher, Halal, Organic, Non-GMO Certified, Identity Preserved, Gluten-free, and others as needed., • Ensures compliance with Mock Recall and item traceability requirements (FDA/customer) including running trace exercises and maintaining company knowledge and resources to perform, • Assist Sales, Legal Team, International Sales, and International Quality teams with regulatory and technical inquiries, certificates, advice and program knowledge, • All other duties as assigned. Qualifications: • Bachelor’s degree in Food Science, Chemistry, Biology or related field with at least 5 years of relevant food manufacturing experience is required., • Familiarity with current good manufacturing practices and food regulation is required., • Prior experience with labeling and claims., • Six Sigma or process improvement experience and SQF practitioner certification desired., • Excellent attention to detail, • Familiar with FSMA requirements, • Previous leadership experience, • Process improvement skills (e.g. Six Sigma), • Proficient command of English and strong communication skills required – both verbal and written., • Must work well in a team environment and have strong communication skills, • Must have the ability to perform under pressure and communicate well with all departments, • Must have good computer skills, including proficiency with Microsoft Excel and Word Physical Demands: • Must be able to physically perform the functions of climbing, balancing, stooping, kneeling, crouching, reaching, standing, walking, pushing, pulling, lifting, grasping, feeling, talking, hearing, and repetitive motions, • Must be able to work seated using a computer and phone for long periods of time., • Must be available to work during extended or off-hours, • Must possess visual acuity to document company records, • Continuous walking throughout plant and distribution center., • Lifting up to 40 pounds

Job Description Company: Davey Resource Group, Inc. Locations: Indianapolis, IN, South Bend, IN Additional Locations: NA Work Site: Hybrid Req ID: 212455 Position Overview DAVEY RESOURCE GROUP, Inc., has openings throughout South Bend, Indianapolis, and the Great Lakes region for experienced environmental consulting professionals. We are seeking teamwork-oriented individuals with excellent written and oral communication skills. Candidates should possess a professional work ethic with attention to detail and safety. Position Description and Responsibilities Selected candidates will work collaboratively with Davey Resource Group project developers, biologists, and project managers on a variety of ecological restoration projects. The position involves preparing and supervising client proposals, technical report writing, and plan development for ecological restoration of upland, wetland and stream environments. Additional experience in environmental planning, permitting, monitoring, construction, wetland delineation and section 401/404 permitting is also a plus. The primary focus of this position is to not only provide senior level project management and expertise, but also perform a key role in the development of new projects, grant writing, networking and identifying new client relationships and project opportunities. This may include attending conferences/workshops and public speaking. Required Qualifications • Minimum of a four-year degree in biology, ecology, conservation, environmental science, or related fields., • At least eight years of experience working in the natural resources field performing ecological consulting work., • Proficient with state laws and environmental regulations., • Valid driver's license and have a good driving record The successful candidate will demonstrate proficiency with stream/wetlands restoration design work, including modeling and plan development; have experience performing construction oversight of restoration projects; be capable of managing large projects with multiple subcontractors; and maintain an existing network of clients and contacts within the ecological consulting industry. Additional Information What We Offer:* • Paid time off and paid holidays., • Opportunities for advancement., • All job specific equipment and safety gear provided., • 401(k) retirement savings plan with a company match., • Employee-owned company and discounted stock purchase options., • Group Health Plan., • Employee Referral Bonus Program: Send-A-Friend., • Locations throughout the United States in major cities and desirable areas., • Career Development Program supported by industry expert safety specialists and skilled trainers., • The Davey Tree Family Scholarship for children of employees. What We Offer:* • Paid time off and paid holidays., • Opportunities for advancement., • All job specific equipment and safety gear provided., • 401(k) retirement savings plan with a company match., • Employee-owned company and discounted stock purchase options., • Group Health Plan., • Employee Referral Bonus Program: Send-A-Friend., • Locations throughout the United States in major cities and desirable areas., • Career Development Program supported by industry expert safety specialists and skilled trainers., • The Davey Tree Family Scholarship for children of employees. Davey Resource Group, Inc., is a leader in the natural resource, environmental, and forestry consulting industries throughout the United States. The Davey Tree Expert Company provides research-driven tree services, grounds maintenance and environmental consulting for residential, utility, commercial and environmental partners in the U.S. and Canada. We care about our clients, each other and the world around us. We offer the resources, size and stability of a big company while maintaining the culture, entrepreneurial spirit and feel of a small one. We invest in our employees by offering industry-leading training, technology and benefits that lead to a rewarding and safe work experience at all levels. Wherever you want to grow your career, there’s a place for you at Davey. To learn more, visit Davey.com. Accommodations: If requested by employee or otherwise as required by law, reasonable accommodations will be made to enable employees with disabilities to perform essential job functions. If you need assistance at any time, please contact us at 1-877-411-7601 or at . Employment Type: Permanent Job Type: Full Time Travel Expectations: Up to 50%

Job Description We are seeking a Laboratory Technician to join the company, a premier supplier, in Indianapolis, IN US While working in this clean, and climate-controlled facility you will have the opportunity to be directly involved in the evolution of the industry. Come work for a company that has been consistently recognized among the Best & Brightest Companies to Work For. Immediate interviews are available, apply today! Job Description: Under the direction of scientists and technicians, the contractor is responsible for supporting the Microbial Repository. Under supervision, the contractor is expected to perform routine and non-routine tasks including but not limited to ordering supplies, cleaning and organizing lab areas, performing manual liquid transfers, operating automated liquid handlers, and storing and retrieving samples from freezers and shakers. The contractor will be responsible for picking samples from freezers for delivery to customers. Given a lighter workload in the Microbial Repository, the contractor may be expected to support activities and complete assigned tasks in other laboratories. The ideal candidate needs to be able to collaborate closely with the Microbial Repository technicians and scientists and complete tasks under their supervision to ensure effective day-to-day operations. • Good communication and time management skills are essential to this role., • Prior experience in microbiology, biotechnology, biology, or related field are required., • Prior experience using aseptic technique is required., • Prior experience with automation is a plus. Critical Success Factors for this role 1. Excellent organizational skills, 2. Aseptic Technique, 3. Strong attention to detail The Company is an Equal Opportunity Employer and is committed to creating an equitable and inclusive environment for all. Company DescriptionWith almost four decades of experience as a proven industry leader, Acro continues to be consistently recognized among the Best & Brightest Companies to Work for in the United States. As an international professional services firm with deep expertise in consulting and staff augmentation offering a variety of solutions including MSP, VMS, RPO, HRO (and more), Acro operates across North America, Europe, and Asia from over 30 locations. Acro’s client portfolio includes some of the most well-known names in business and provides services across all verticals including technology, aerospace, energy, automotive, government, and manufacturing. To learn more, please visit almost four decades of experience as a proven industry leader, Acro continues to be consistently recognized among the Best & Brightest Companies to Work for in the United States. As an international professional services firm with deep expertise in consulting and staff augmentation offering a variety of solutions including MSP, VMS, RPO, HRO (and more), Acro operates across North America, Europe, and Asia from over 30 locations. Acro’s client portfolio includes some of the most well-known names in business and provides services across all verticals including technology, aerospace, energy, automotive, government, and manufacturing. To learn more, please visit .

Job DescriptionSalary: Head of Structural Biology Helix BioStructures, LLC (HBS) is a contract research organization based in Indianapolis, Indiana, providing early drug discovery services to the biopharmaceutical industry. HBS maintains a full suite of services that encompass chemical & structural analysis, protein production, computational modeling, and design. HBSs core and most popular services are structural biology techniques, X-ray Crystallography, and Cryo-EM. HBS was founded in 2018 and has grown considerably. We are looking to add an experienced Head of Structural Biology to our Indianapolis-based team. Main Responsibilities This role will lead, manage, and support the Helix team, planning & tracking all projects to produce high-quality work and support our clients projects. A proven track record in managing people and projects with a deep understanding of protein construct design, expression, and purification of challenging proteins, biophysical characterization, and structural biology techniques is essential. Highly desirable scientific knowledge and hands-on experiences include: Protein Production Across Multiple Systems: Extensive experience with protein production in various cell lines, including bacteria, insect, mammalian, and yeast. Expertise in optimizing expression and purification strategies for diverse and challenging proteins. Biophysical Characterization: Proficiency in biochemical, biophysical, and structural characterization of proteins. Protein Crystallography: Extensive experience in crystallizing proteins and/or nucleic acids, with a deep understanding of structure solution and refinement. Cryo-EM: Skilled in cryo-EM grid preparation, data collection, and processing, with experience in tackling complex and challenging projects. Leadership and Project Management: Demonstrated ability to lead and manage projects, teams, and employees effectively, ensuring alignment with business goals and successful project outcomes. Ability to mentor and develop team members, driving both individual and organizational growth. In addition to expertise in protein biochemistry and structural biology, this role will provide a range of experimental strategies (biochemical, biophysical, and/or computational) to support our clients needs. Accordingly, proficiency in protein production and structural biology is essential. The successful candidate will have a deep scientific understanding and can plan and lead the team and multiple projects in parallel. Overall, you will be an outstanding project and people leader who will significantly impact our gene-to-structure service portfolios with the unique opportunity to help drive our business. Additional Responsibilities Create and manage necessary documents and communicate research priorities, progress, and results to clients/project teams and upper management. Provide the team with project details and priorities, technical and scientific guidance, deliverables, and timelines. The candidate will be responsible for managing the team and all projects, providing support, including necessary bench work for project success. The candidate will manage his/her direct reports and provide the support needed. The candidate will be responsible for making sure Helixs clients receive timely updates on project statuses. Required Qualifications Ph.D. in biochemistry, biophysics, protein engineering, and/or structural biology. Industry experience: 3-7 years post-Ph.D. (not including time as an academic postdoc). Demonstrated experience and knowledge in people and project management. Demonstrated knowledge of construct design for structural/biophysical studies. Demonstrated experience and knowledge in protein expression and purification strategies using bacterial, insect, mammalian, and yeast cell lines. Demonstrated experience and knowledge of structural biology, including X-ray Crystallography and Cryo-EM. Strong leadership, written and oral communication skills, and attention to detail. Location This position is based in Indianapolis, Indiana, and does NOT offer a hybrid option. Interaction with external service vendors is also expected. Physical Requirements Able to lift 30 lbs objects. Able to visualize microscopic objects under microscopes. Non-standard Work Schedule, Travel, and Lab Safety Able to adhere to safe work practices and perform lab work with appropriate personal protective equipment such as but not limited to safety goggles, facial mask, gloves, lab coat/protective gowning, and closed-toe shoes. Able to work flexible hours occasionally when performing time-sensitive experiments. Other Job Details Eligible for Relocation Support Competitive Salary + Bonus Competitive Paid Time Off Retirement (matching 401K) Health/Dental/Vision Insurance Company Computer Helix BioStructures, LLC is an equal-opportunity employer, and we embrace the increasingly diverse world around us. Helix BioStructures, LLC prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin or ancestry, age, disability, marital status, and veteran status.

Job Description Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: Key Responsibilities: • Develop and maintain the Contamination Control Strategy (CCS) in alignment with EU Annex 1, FDA Guidance, and industry best practices., • Provide technical oversight for aseptic processing, cleanroom qualification, and sterilization processes (e.g., moist heat, dry heat, radiation, filtration)., • Lead and support media fill (aseptic process simulation) planning, execution, and evaluation., • Review and approve environmental monitoring (EM) and cleanroom classification protocols and data trends., • Serve as the subject matter expert (SME) during regulatory inspections and internal audits related to sterility assurance., • Evaluate and recommend improvements in facility design, airflow patterns, and personnel/material flow for aseptic areas., • Provide input into the design qualification and validation of sterilizers, cleanroom HVAC systems, isolators, RABS, and barrier technologies., • Participate in deviation investigations, CAPAs, and risk assessments involving microbiological contamination or sterility failures., • Author and maintain SOPs, risk assessments, protocols, and reports related to sterility assurance., • Support training programs for aseptic technique, gowning, and microbiological control., • Collaborate with Quality, Validation, Engineering, and Manufacturing to ensure a holistic approach to sterility assurance. Required Qualifications: • Bachelor’s or Master’s degree in Microbiology, Biology, Pharmacy, Biotechnology, or related field., • 5+ years of experience in a GMP-regulated environment, preferably in aseptic processing or microbiology QA/QC., • In-depth knowledge of GMP, USP <71>, <85>, <1116>, EU Annex 1, ISO 14644, and PDA technical reports., • Experience with cleanroom operations, aseptic technique, sterilization methods, and EM programs., • Strong problem-solving, risk assessment, and technical writing skills., • Excellent communication skills and ability to work cross-functionally. Preferred Qualifications: • Experience with isolator technology or advanced aseptic processing (e.g., closed RABS, automated filling lines)., • Knowledge of terminal sterilization validation, biological indicators, and sterility test validation., • Familiarity with Lean/Six Sigma or Quality by Design (QbD) principles in sterility assurance., • Prior participation in regulatory inspections (FDA, EMA, MHRA, etc.) as SME.

Job DescriptionSalary: Cogent Scientific, an insourced contract research organization in Indianapolis, is looking for the right people to accomplish our Mission: partnering in the global effort to improve lives through innovative science with an experienced workforce. We typically hire scientists with the following backgrounds: • BS/MS - Chemistry, Biochemistry, Organic Chemistry, Molecular Biology and related fields., • Industrial experience in pharma/biotech arenas., • Laboratory skills sets such as: organic synthesis, purification and formulation; analytical chemistry utilizing LC, LC/MS, wet chemistry techniques; molecular biology using PCR, cell culture, Western blot., • Team players who embody our Core Values:, • Client Focused: We only succeed when our clients succeed., • Outstanding: We deliver meticulous results through outstanding performance., • Good: We act ethically and morally., • Employee-Centric: We honor and support our employees., • Nimble: We are prepared to adapt in an ever-changing industry., • Team-Oriented: We collaborate with each other and with our clients. If you do not see a job posted on our employment page that fills your skills and experience, feel free to upload your information and resume here. We are continually growing and look forward to working with you soon!

Job Description Job Duties/Responsibilities: Work environment/department will be listed in requirement. Determine the acceptability of specimens for testing according to established criteria. Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. Monitor, operate and troubleshoot instrumentation to ensure proper functionality. Demonstrate the ability to make technical decisions regarding testing and problem solving. Prepare, test, and evaluate new reagents or controls. Report accurate and timely test results to deliver quality patient care. Perform and document preventive maintenance and quality control procedures. Identify and replenish testing bench supplies as necessary. Assist with processing of specimens when needed. Maintain a safe work environment and wear appropriate personal protective equipment Requirements: Associate degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements. Minimum 2-4 years of clinical laboratory testing experience is required. State Medical Technician license may be required (will be listed in requirement if its needed). ASCP or AMT certification is either preferred or required (will be listed in requirement if its required). Ability to work independently and within a team environment. Proficient with computers; Familiarity with laboratory information systems is a plus. High level of attention detail along with strong communication and organizational skills. Must be able to pass a standardized color vision screen. Flexibility to work overtime or other shifts depending on business needs

Job Description VitaCyte is a leading manufacturer of purified-defined bacterial collagenase and associated protease enzymes for enzyme-mediated cell isolation and other biotherapeutic applications. The company has established a Quality Management System (QMS) to comply with ISO-9001 and aligned with industry standards and regulations. • Job Purpose, • Maintain the QMS to ensure compliance with ISO 9001 and applicable regulatory standards in a state of inspection readiness under the direction of the Director of Quality Assurance., • Duties & Responsibilities, • Ensures VitaCyte personnel comply with an ISO 9001 certified QMS and applicable regulatory requirements., • Owns and delivers the training program for the site while ensuring compliance with the QMS and applicable regulatory requirements. Management of the training program may include facilitation of course creation & revision, course instruction & remediation, coordination of the training schedule, maintaining employee training files, and periodic metrics trending and reporting., • Owns the site inspection readiness program, which includes periodic self-assessments, customer audits, and external agency inspections. Management of the inspection readiness program includes but is not limited to the facilitation of inspection planning, executing, reporting, appropriate escalation/notification to management, closing & executive summaries, and tracking and evaluating the effectiveness of any performed remediation by the audited party., • Owns and executes the vendor management program for the site while ensuring compliance with the QMS and applicable regulatory requirements. Vendor management may include negotiating terms of Quality Assurance Agreements, creation & revision of the vendor management procedure & risk classification procedure, vendor inspections, vendor classifications, onboarding, performance monitoring, metric reporting, and termination., • Owns the non-conformance management process, which includes deviation, corrective actions, root cause investigations, and documentation management, • Support equipment and facility maintenance and calibration records, • Support change management processes and records, • Qualifications, • Education/Experience, • Bachelor’s Degree in Chemistry, Biochemistry, Biology, or Biotechnology, or related field, • Minimum 3-years experience working with a quality management system, • Knowledge of applicable standards and regulations (ex. ISO 9001, ICH Q7, 21 CFR Part 210/211), • Maintaining ISO certification is preferred., • Experience with eQMS and/or CMMS software preferred., • Auditing experience preferred., • Skills/Abilities, • Comfortable working in a laboratory environment including lab safety, general chemical knowledge, clean room attire and recording results in controlled documents, • Strong computer skills including comfort using web-based software tools, • Strong documentation, interpersonal, communication and problem-solving skills while working in a team environment, • Average physical strength and ability to stand for long periods, • Benefits, • Full time, permanent position including a comprehensive family medical benefit package and participation in an employer matched 401K plan., • Salary is commensurate with experience.

Job Description The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures. WORKING AT GENEZEN Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team. JOB SUMMARY Responsible for leading routine performance of downstream manufacturing operations including advanced laboratory techniques related to viral vector production and analytics as well as basic laboratory functions. Responsibilities and laboratory techniques required for this position include aseptic technique, preparing solutions and media, molecular biology techniques, cell culture techniques, and general cleanroom sanitization/area maintenance. The position requires working both independently and serving as the manufacturing Downstream SME for client processes, but also under the supervision of the Manufacturing Manager. ESSENTIAL JOB FUNCTIONS • Serve as the lead Downstream operator for coordinating team responsibilities and peforming hands on manufacturing processes related to viral vector production including downstream manufacturing tasks under the guidelines of established procedures and batch records, • Lead manufacturing activities within a team environment related to clarification, chromatography, TFF and filling activities, • Serve as a liason with downstream process development SMEs to understand the latest downstream process development processes/practices and ensure feasibility of translation of said processes/practices to a GMP manufacturing environment, • Maintain manufacturing material supply, primarily ensuring manufacturing spaces are adequately stocked and prepared, • Assist in the maintenance of laboratory equipment and laboratory support operations, • Lead in the creation, review, and revision of SOPs, batch records, and forms in coordination with management, PD and Quality Assurance, • Ensure roles and responsibilities for executing downstream manufacturing processes are clear to the operators assigned to the processes and assist with coaching/training operators as needed, • Follow detailed instructions with a high level of focus and attention to detail, • Complete documentation accurately and in a timely fashion, • Maintain up to date training status, • Use, clean, and maintain laboratory spaces and manufacturing equipment, • Lead in troubleshooting of downstream manufacturing issues, with assistance from Manufacturing Management as needed, • Train new staff members and fellow employees in all relevant downstream manufacturing processes, • Comply with all established policies and SOPs, • Perform safety inspections and maintain a safe working environment, • Use industrial equipment such as pallet jacks, • Perform area sanitization and collect/dispose of waste per established procedures, • Help collect process data for metrics/trending, • Assist in tasks required to be performed in a BSL-1, -2, or -3 environment., • Contribute to the support, optimization, and improvements of GMP products, • Assist in specification development and review via Corrective and Preventive Actions (CAPA) and/or change controls, • Adaptability required as work schedule may change based on business needs, • Criminal background check required EDUCATION / CERTIFICATIONS / LICENSES Essential/Desired BS degree in Biology, Biochemistry, Molecular Biology, or similar field Essential ON-THE-JOB EXPERIENCE Minimum 2 years of post-graduation experience in a GMP environment Essential 2 years of experience operating in a GMP laboratory using aseptic technique and risk mitigation strategies Essential 2 years of experience with at scale Clarification, Chromatography, and TFF platforms Essential Experience in cell and gene therapy DS/DP manufacturing, specifically viral vectors Strongly Desired SKILLS / ABILITIES Excellent computer, verbal, and written communication skills Essential Ability to work independently with minimal supervision as well as within in a team, specifically as the lead operator during manufacturing activities Essential Able to adapt quickly to changing ideas, responsibilities, strategies, and other processes Essential Willing to work in an environment where individual initiative, collaboration, and accountability are valued Essential PHYSICAL DEMANDS While performing the duties of this job, the employee is required to meet the following physical demands: Work Environment • Frequently required to work in a BSL 2 environment with personal protective equipment/aseptic gowning, • Regularly required to work around large machinery and typical utilities seen in pharmaceutical facilities, • Occasionally exposed to moving mechanical parts; high, precarious places; toxic or caustic chemicals; hazardous waste; and risk of electrical shock, • Frequently required to stand; sit; walk; balance; stoop; kneel; crouch; use hands to finger, handle, or feel; reach with hands and arms, • Frequently lift and/or move up to 25 pounds, • Frequently required to communicate by talking, hearing, using telephone and e-mail GENEZEN'S CURES VALUE-BASED COMPETENCIES Committed to Science We are committed to scientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare. Urgency in action for the patients We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs. Resilience & Grit in operations We are committed to overcoming challenges, learning from failures, and persistently striving for success. Execute with Excellence & Integrity We are dedicated to delivering quality results and upholding ethical principals. Solutions driven for our partners We are committed to being a proactive, collaborative, creative and open-minded partner. GENEZEN'S BENEFITS • Paid vacation days, amount based on tenure, • Paid sick time, • 10 observed holidays + 2 floating holiday + 1 volunteer day, • 401(k) plan with company match up to 6% of salary, vested immediately, • Share Appreciation Rights, • Choice of several healthcare plans, • FSA and HSA programs, • Dental & vision care, • Employer-paid basic term life/personal accident insurance, • Voluntary disability, universal life/personal accident insurance, • Nothing in the job description for this role restricts management's right to assign or reassign duties and responsibilities to this job at any time., • This position requires a criminal background check., • Genezen is an Equal Opportunity Employer., • Genezen participates in EVerify. Fishers is a suburb of Indianapolis. Fishers was named the #1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world's largest children's museum--to name just a few reasons why this area is a great place to live. Lexington, Massachusetts, located just northwest of Boston, is renowned as a historic suburb with a rich cultural heritage. It boasts picturesque New England charm, tree-lined streets, and a vibrant community. Known for its pivotal role in the American Revolution, Lexington offers visitors and residents alike a blend of historical landmarks, modern amenities, and a strong sense of community pride.

Pride Health is hiring a Medical Laboratory Scientist to support our client’s medical facility based in Indianapolis, IN 46214. This is a Contract job with a possible extension opportunity and a great way to start working with a top-tier healthcare organization! Location: Indianapolis, IN 46214 Job Type: 12+ Months - W2 contract - with possible extension Schedule: 2nd Shift (United States of America) - USA_2_Shift Pay Range: $30-$36/hr. (Offered pay rate will be based on education, experience, and healthcare credentials.) Responsibilities: Responsibilities are interchangeable within job titles of medical laboratory scientist (MLS), medical technologist or clinical laboratory scientist. Work environment/department will be listed in requirement. Determine the acceptability of specimens for testing according to established criteria. Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. Monitor, operate and troubleshoot instrumentation to ensure proper functionality. Demonstrate the ability to make technical decisions regarding testing and problem solving. Prepare, test, and evaluate new reagents or controls. Report accurate and timely test results to deliver quality patient care. Perform and document preventive maintenance and quality control procedures. Identify and replenish testing bench supplies as necessary. Assist with processing of specimens when needed. Maintain a safe work environment and wear appropriate personal protective equipment Requirements: Bachelor’s degree in biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements. Minimum 0-2 years of clinical laboratory testing experience is required. Ability to work independently and within a team environment. Proficient with computers; Familiarity with laboratory information systems is a plus. High level of attention detail along with strong communication and organizational skills. Must be able to pass a standardized color vision screen. Flexibility to work overtime or other shifts depending on business needs Skills required: Pipetting ELISA 96 Well Plating LIS (lab information system) knowledge Education: BACHELOR’S DEGREE IN BIOLOGY OR CHEMISTRY. Pride Global offers eligible employees comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance, and hospital indemnity), 401(k)-retirement savings, life & disability insurance, an employee assistance program, legal support, auto, home insurance, pet insurance, and employee discounts with preferred vendors. About Pride Health Pride Health is Pride Global's healthcare staffing branch, providing recruitment solutions for healthcare professionals and the industry at large since 2010. As a minority-owned business that delivers exceptional service to its clients and candidates by capitalizing on diverse recruiting, account management, and staffing backgrounds, Pride Health's expert team provides tailored and swift sourcing solutions to help connect healthcare talent with their dream jobs. Our personalized approach within the industry shines through as we continue cultivating honest and open relationships with our network of healthcare professionals, creating an unparalleled environment of trust and loyalty. Interested? Apply today!

Job Description Job Duties/Responsibilities: Responsibilities are interchangeable within job titles of medical laboratory scientist (MLS), medical technologist or clinical laboratory scientist. Work environment/department will be listed in requirement. Determine the acceptability of specimens for testing according to established criteria. Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. Monitor, operate and troubleshoot instrumentation to ensure proper functionality. Demonstrate the ability to make technical decisions regarding testing and problem solving. Prepare, test, and evaluate new reagents or controls. Report accurate and timely test results to deliver quality patient care. Perform and document preventive maintenance and quality control procedures. Identify and replenish testing bench supplies as necessary. Assist with processing of specimens when needed. Maintain a safe work environment and wear appropriate personal protective equipment Requirements: Bachelors degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements. Minimum 0-2 years of clinical laboratory testing experience is required. State Medical Technologist license may be required (will be listed in requirement if its needed). ASCP or AMT certification is either preferred or required (will be listed in requirement if its required). Ability to work independently and within a team environment. Proficient with computers; Familiarity with laboratory information systems is a plus. High level of attention detail along with strong communication and organizational skills. Must be able to pass a standardized color vision screen. Flexibility to work overtime or other shifts depending on business needs

Job Description The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures. WORKING AT GENEZEN Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team. JOB SUMMARY Direct the development and establishment of processes in Process Development. This individual is accountable for developing a scalable platform for viral vector production processes that minimizes the risk during Process Development to GMP scale-up. The individual will provide technical expertise and leadership in science & technology and requires close collaboration with internal stakeholders. ESSENTIAL JOB FUNCTIONS • Be accountable for establishing the downstream platform from small scale through intermediate scale (50L) lentiviral and retroviral vector processes., • Responsible for monitoring and reporting on process performance, identifying opportunities, and implementing changes to improve process, product safety, and product quality., • Develop and support process optimization efforts to increase process robustness, reduce costs, and improve viral yield and purity., • Design and execute experiments independently: accurately record, analyze, and communicate data to senior management and team members., • Maintain open communication via one-on-one and team meetings., • Stay current with relevant technologies and needs to be adept at identifying new approaches., • Perform and lead single-use system design manifold, selection, implementation, configurations in between Upstream bioreactor and downstream unit operations and control strategies., • Develop proper SOP for downstream processes, • Responsible for the process transfer from or to clients and to in-house manufacturing plant., • Maintain external technical relationships and collaborate with equipment and material suppliers., • Serve as process SME for regulatory and client audits., • Adaptability required as work schedule may change based on business needs, • Criminal background check required EDUCATION / CERTIFICATIONS / LICENSES Essential/Desired BS, MS, or PhD in biological engineering Desired ON-THE-JOB EXPERIENCE 5-8 years of relevant industry experience Desired Solid foundation in the fundamentals of biochemical engineering, virology and cell biology Essential Entrepreneurial experience dealing with customers in product development Desired Pharmaceutical industry experience in technical support of cGMP manufacturing and/or process development, including experience with Contract Development and Manufacturing Organizations Desired Experience with cell culture technologies, molecular biology, upstream processing, and aseptic processing Desired SKILLS / ABILITIES Solid knowledge of principles of chromatography with AKTA system and Unicorn software and TFF Solid knowledge of principles of aseptic technique Working knowledge of cGMPs related to the production of viral therapeutics Desired Ability to interface successfully with multi-disciplined teams Desired Extremely detail-oriented with strong technical skills & mechanically inclined/knowledge of hand tools Desired PHYSICAL DEMANDS While performing the duties of this job, the employee is required to meet the following physical demands: Work Environment • Frequently required to work in a BSL 2 environment with personal protective equipment/aseptic gowning, • Regularly required to work around large machinery and typical utilities seen in pharmaceutical facilities, • Occasionally exposed to moving mechanical parts; high, precarious places; toxic or caustic chemicals; hazardous waste; and risk of electrical shock, • Occasionally exposed to extremely loud noise levels, • Frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms, • Frequently lift and/or move up to 10 pounds, • Frequently required to communicate by talking, hearing, using telephone and e-mail GENEZEN'S CURES VALUE-BASED COMPETENCIES Committed to Science We are committed to scientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare. Urgency in action for the patients We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs. Resilience & Grit in operations We are committed to overcoming challenges, learning from failures, and persistently striving for success. Execute with Excellence & Integrity We are dedicated to delivering quality results and upholding ethical principals. Solutions driven for our partners We are committed to being a proactive, collaborative, creative and open-minded partner. GENEZEN'S BENEFITS • Paid vacation days, amount based on tenure, • Paid sick time, • 10 observed holidays + 2 floating holiday + 1 volunteer day, • 401(k) plan with company match up to 6% of salary, vested immediately, • Share Appreciation Rights, • Choice of several healthcare plans, • FSA and HSA programs, • Dental & vision care, • Employer-paid basic term life/personal accident insurance, • Voluntary disability, universal life/personal accident insurance, • Nothing in the job description for this role restricts management's right to assign or reassign duties and responsibilities to this job at any time., • This position requires a criminal background check., • Genezen is an Equal Opportunity Employer., • Genezen participates in EVerify. Fishers is a suburb of Indianapolis. Fishers was named the #1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world's largest children's museum--to name just a few reasons why this area is a great place to live. Lexington, Massachusetts, located just northwest of Boston, is renowned as a historic suburb with a rich cultural heritage. It boasts picturesque New England charm, tree-lined streets, and a vibrant community. Known for its pivotal role in the American Revolution, Lexington offers visitors and residents alike a blend of historical landmarks, modern amenities, and a strong sense of community pride.

Shift: Monday through Friday 8:00 AM - 4:30 PM Are you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives. Compensation: $22.00 - $25.00 per hour Candidate will use their skills and knowledge in Microbiology, Molecular Biology and Bacteriology to support development of new products. What you'll do: * Manipulate microbial genetic material for the development of new products * Conduct analysis of pharmaceutical products using traditional microbiological techniques such as dilution, pour plating, and filtration * Under the direction of lab management, perform a wide range of general Microbiology and Molecular testing to include: PCR, PCR design, primer design, PCR optimization, DNA extraction from bacteria, * DNA sequencing, DNA gel electrophoresis, protein extraction, BCA assay, PAGE, Western blotting, Western blot optimization, Silver staining, antibody sourcing, bacteriology and fermentation * May also perform: cloning, subcloning, restriction digests, ligations, transformations, Southern blots and protein expression * Culturing bacterial and mammalian cell lines What you'll Bring: * Bachelor's degree in Biology, focus in Microbiology and Molecular Biology preferred * Understanding of the microbiology and molecular testing - Sterile Technique experience * Mammalian Cell Culture experience, Required * Able to perform testing to SOP specifications * Highly organized with and attentive to detail * Strong communication and lab documentation/reporting skills Find Your Place at Pace - We need you - your curiosity, your talents, and your drive - to help us advance this important work. Benefits When you join Pace , you commit to work that makes a positive impact on our communities and our world. We commit to supporting you with benefits and perks that make a positive impact on your life. Full-time roles are eligible for our comprehensive benefits program which includes competitive salaries, medical, dental vision, 401K retirement savings plan (100% vested immediately in the employer match), life, disability and voluntary benefits, paid time off for holiday, sick and vacation days, HSA, wellness program, flexible spending accounts, tuition reimbursement, Employee Assistance program, parental leave, optional legal coverage and ID theft. Equal Opportunity Employer Pace provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, 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.

Job Description The Indianapolis Zoo's Primates department is searching for a keeper to join our growing team! This position will primarily care for our chimpanzee, orangutan, baboon, gibbon, macaque, and tamarin residents. Duties include cleaning and maintaining animal environments, preparing and distributing daily enrichment, observing animal behavior, participating in positive reinforcement training, ensuring optimal animal welfare, supporting a variety of research activities, and educating zoo guests. The ideal candidate is committed to advancing the Zoo's mission to protect nature and inspire people to care for our world. Prior experience in the animal care profession, preferably a zoological setting, is required. Prior experience working with Primates is highly desired. This is a full-time, 40 hours per week position that requires availability to work weekends, holidays, and overtime as needed. Strong observational and communication skills (both verbal and written), as well as a team-oriented attitude are essential. Working with Primates requires a specialized skillset and physical abilities that include but are not limited to: • One (1) year of prior related work experience., • Bachelor's degree from an accredited college/ university in Zoology, Biology, or a related field is required., • Demonstrates patience, gentleness, respect, and consistency with animals in their care., • Assists with developing and implementing area chats, feeds, demonstrations and behind the scenes tours., • Completes daily husbandry tasks and recordkeeping., • Assists with exhibit modifications and repairs. Previous experience with tools is desirable., • Displays a professional attitude and appearance to visitors, volunteers, and co-workers., • Ability to transport and move items, exerting up to 100 pounds of force occasionally, and up to 50 pounds of force frequently., • Ability to ascend/ descend ladders, steps and uneven terrain, while maintaining body equilibrium to perform various jobs., • Ability to work comfortably at heights, and operate a scissor lift as necessary., • Ability to detect, assess, identify, and observe surroundings to make sound judgments, along with the ability to communicate verbally, comprehend and decipher information accurately, using a two-way radio and telephone., • Valid driver's license and driving record that is insurable by our carrier. To apply: • Interested candidates must complete an online Zoo application., • Interested candidates must include a resumé, cover letter, and salary requirements to be considered. Employment at the Indianapolis Zoo is contingent upon the successful completion of pre-employment testing including a background check, motor vehicle check (if applicable) and a drug test. Job Posted by ApplicantPro

BC Forward is hiring for CPD&D Laboratory Technician at Indianapolis, IN Position: CPD&D Laboratory Technician Location: 9330 Zionsville Road, Indianapolis, IN 46268 Duration: 11 Months (Possible Extension) Work type: Onsite Shift Times: 8:00am - 4:30pm | Mon-Fri Pay Rate: $21.50/hr Description: Any specific skills, requirements or experience you want in a candidate: Experience in Entomology & with nematodes and insects; BS Degree Preferred. Recent Grads Okay. Notes: • Looking a for a candidate with a degree in Biology with a focus on Entomology and/or Nematology., • Candidate will be using chemical spray., • Standing for long periods of time, • PPE for laboratory and spraying is provided by employer. Job Description: Wanted: individual capable of working with insects, plant material, and nematodes while completing routine, highly detailed work. Previous laboratory experience preferred. Work environments vary throughout the day between laboratory, greenhouse, and insectary colonies. Strong culture of safety requires individuals to adhere to all safety and ergonomic standards. Extensive training in safety, ergonomics, and laboratory SOPs provided. Basic tasks may include: • Clipping/thinning plants used in testing., • Hands-on infesting of plant and artificial diet material with various (non-stinging, non-hazardous) insect species., • Routine assay formulation using manual pipettes., • Specialized assay application using hand sprayers and track sprayers., • Laboratory maintenance (cleaning, restocking, etc.)., • Grading insect assays., • Preparation of media used in entomology testing., • Scribing for evaluators Requirements: • Self-driven individual that also works well in a diverse group setting., • Flexibility to shift focus throughout the day as needed to meet customer demands., • Willing to work independently and with a team as needed. Self-initiated and desire to learn. • Strong communication and time management skills, • Ability to follow directions and protocols, • Must have work experience* Does not need to be related to lab work, but must have had any job previously. 1. Educational Requirements: § BS in Biology/Entomology 2. Safety and Compliance: Adherence to Corteva Safety Protocols: Understands and follows EH&S standards. Use of safety procedures & appropriate PPE mandated. Compliance with laboratory safety procedures. 3. Soft Skills: Communication and Collaboration: Strong written and verbal communication skills, effective documentation and communication of results, good organization skills, follow SOPs, and adhere to safety protocols, strong interpersonal and collaboration skills.

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: The Production Technician, Processing will utilize experience and training to manufacture pharmaceuticals in a strictly controlled GMP environment. The employee will progress through several job functions and be required to demonstrate increasing skill levels. Responsibilities include but are not limited to: \n • Comply with all Company and GMP compliance policies/procedures.\n, • Perform area sanitization procedures in a GMP Manufacturing facility.\n, • Perform filter integrity testing.\n, • Clean miscellaneous pieces of manufacturing equipment and vessels.\n, • Perform raw material weighing (dispensing) and bulk formulation.\n, • Assist PT3 operators as instructed.\n, • Perform system maintenance PM's and procedures.\n, • Perform sterile filtrations, unload the autoclave, and complete Steam-in-Place operations.\n, • Assist in training/directing PT1 operators.\n, • Attend mandatory annual hazardous waste training meeting(s) and demonstrate competency in that training by passing test(s) administered by the company or consultant providing such training. Must immediately notify supervisor if affected by infectious disease or open lesions on body, as individuals are not permitted to enter manufacturing areas or handle product if these conditions exist.\n, • 2-2-3 Schedule: 7am - 7pm\n\n Physical Attributes: \n • Frequent standing, walking, and sitting.\n, • Stoop, kneel, bend, crouch, or crawl, talk or hear on occasion.\n, • Lift and/or move up to 25 pounds.\n\n Who You Are: Minimum Qualifications: \n • High School Diploma or GED.\n, • 3+ years' work experience Good Manufacturing Practices (GMP) in a regulated manufacturing facility.\n\n Preferred Qualifications: \n • Bachelor's Degree in Chemistry, Biology, Biochemistry, or other Life Science discipline.\n, • Experience reading, comprehending, and discussing detailed GMP documentation.\n, • Experience in bulk formulation along with equipment cleaning, preparation, and assembly.\n\n Pay Range for this position: $26 - $40 / hour The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Job Description Outreach Biologist Assistant The International Crane Foundation (ICF) is seeking a passionate and driven Outreach Biologist Assistant to join our team in Western or Central Indiana. This position plays a vital role in advancing ICF's mission to conserve cranes and the ecosystems, watersheds, and flyways they depend on. Focusing on areas near key crane habitats including Jasper-Pulaski and Goose Pond Fish and Wildlife Areas, the Outreach Biologist Assistant will lead community engagement efforts, build local partnerships, support volunteer coordination, and contribute to essential conservation research-specifically focused on Whooping Cranes and Sandhill Cranes. This full-time, hourly position has an ideal start date at the end of October and pays $19.00 an hour. In addition to a base hourly wage, we offer a comprehensive benefits package that includes health, dental, and vision insurance, 401(k) with employer contributions, generous paid time off, and additional perks designed to support work-life balance and well-being. About the Role This is a unique opportunity for a biologist who thrives at the intersection of science and public engagement. You will represent ICF in communities across Western Indiana, developing and delivering in-person and virtual programs for diverse audiences including hunting groups, birders, civic organizations, zoos, and landowners. You will also play a key role in raising awareness about Whooping Cranes through public speaking, naturalist programs, media interviews, and social media content. Beyond outreach, your work will support the long-term survival of these endangered birds through hands-on conservation research. This includes monitoring crane behavior and habitat use, conducting field surveys using radio telemetry, and gathering data at key sites, including areas where new solar energy developments intersect with crane habitats. You'll also assist in data entry and contribute to reports and scientific publications that inform broader conservation strategies. Collaboration is at the heart of this role. You'll work closely with ICF's Whooping Crane Project Manager and coordinate with our outreach teams in Wisconsin and Alabama. You'll also form critical relationships with landowners, volunteers, and local partners who help watch over and protect cranes in their communities. Managing and mentoring volunteers is a core part of the role, as is training them to extend the reach of ICF's educational programs. Qualifications We are looking for candidates with a bachelor's degree in biology, wildlife conservation, or a related field, who bring experience in public speaking, landowner and volunteer engagement, and field data collection. You should be comfortable using Microsoft Office tools and online platforms like Zoom and Microsoft Teams to engage remote audiences. A valid driver's license and reliable vehicle are required, and travel expenses will be reimbursed. If you're excited by the idea of combining science, education, and community engagement to protect one of North America's rarest birds, we encourage you to apply. This is more than a job-it's a chance to make a lasting impact in the conservation of iconic species and their habitats. Join us in Western Indiana and help cranes thrive into the future. How to Apply: Go to to learn more about ICF and this position and to apply quickly. The deadline for applications is 10/14/2025. Job Posted by ApplicantPro

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Looking a for a candidate with a degree in Biology with a focus on Entomology and/or Nematology.

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