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Essential Functions and Responsibilities: • Evaluates the chemical and physical properties of various substances, • Follows the instructions and pre-established guidelines to perform the functions of the job, • Responsible for routine chemical analysis work and reviewing involving pharmaceutical raw materials, process intermediates and finished products following GMPs, • Prepare volumetric test solutions and mobile phases, • Utilize knowledge of High-Performance Liquid Chromatography (HPLC), Inductively Coupled Plasma (ICP), and titration techniques., • Maintains appropriate documentation (records and lab notebooks) as required by SOP’s and cGLP’s, • Audits raw data results and laboratory documentation, • Calculates, interprets and review test results. Prepare test reports and review lab notebooks, • Performs OOS investigations as described in the SOPs to establish integrity of data Phase I & Pase II), • Operates, maintains, calibrates and qualifies equipment in assigned areas, • Able to write and execute protocols with minimum supervision and SOPs, • Assist in investigations, development and validation to method development., • Disposes waste according to Environmental Protection Agency (EPA) regulations and transfer of gas cylinders, • Follows laboratory safety rules, • Assists in the process of methods development, • Other duties as assigned by the immediate Supervisor Qualifications: • Bachelor’s degree in Chemist or Science discipline and/or equivalent work experience, • 1 - 3 years experience, • Bilingual (English and Spanish) preferred, • Basic use of Excel, Word and quality management systems., • Knowledge of lab equipment (HPLC, ICP-MS, GC, UV, FT NIR), • Experience and knowledge in Methods Validation, • Knowledge in GMP regulations and safety practices, • Knowledge of GLP practices.

Job Description Essential Functions and Responsibilities: • Evaluates the chemical and physical properties of various substances, • Follows the instructions and pre-established guidelines to perform the functions of the job, • Responsible for routine chemical analysis work and reviewing involving pharmaceutical raw materials, semi-finished goods, and finished goods according to defined specifications, • Performs a variety of laboratory techniques including sample weighing and recording preparation of standard solutions, buffers, sample preparation requiring extractions, filtration, centrifugation, pipetting, etc., • Audits raw data results and laboratory documentation, • Calculates, interprets, and reviews test results. Prepares test reports and reviews lab notebooks, • Performs OOS investigations as described in the SOPs to establish integrity of data, • Operates, maintains, calibrates and qualifies equipment in assigned areas, • Ability to write and execute protocols with minimum supervision and SOPs, • Follows laboratory safety rules, • Assists in the process of methods development, • Bachelor’s degree in Chemistry or related, • 1 - 3 years’ experience as Industrial Chemist, • Bilingual (English and Spanish), • Knowledge in lab equipment (HPLC, ICP/MS, UV, IR), • Knowledge in GMP and GLP regulations

Job Description Job Title: Industrial Chemist (2nd Shift) Location: Davie, FL Schedule: Monday to Friday, 4:15 PM – 12:45 AM Position Summary: We are seeking a motivated Industrial Chemist to join our pharmaceutical manufacturing team on the 2nd shift. The ideal candidate will have a strong background in analytical chemistry and experience working in a GMP-regulated environment. This role is responsible for performing chemical analyses on raw materials, intermediates, and finished products to ensure quality and compliance. Essential Functions & Responsibilities: • Evaluate the chemical and physical properties of various substances using analytical techniques, • Perform routine chemical analysis of pharmaceutical raw materials, intermediates, and finished products in compliance with GMP standards, • Follow pre-established protocols and SOPs to carry out lab functions accurately, • Audit raw data, results, and laboratory documentation for accuracy and completeness, • Calculate, interpret, and review test results; prepare reports and maintain detailed lab notebooks, • Conduct Out-of-Specification (OOS) investigations per SOPs to ensure data integrity, • Operate, maintain, calibrate, and qualify laboratory instruments in assigned areas, • Assist with method development and protocol execution with minimal supervision, • Adhere to all laboratory safety protocols and company policiesQualifications:, • Bachelor’s degree in Chemistry or related field, • 1–3 years of experience in a pharmaceutical manufacturing or analytical lab setting, • Bilingual in English and Spanish (preferred), • Hands-on experience with lab instruments such as HPLC, GC, UV, and IR, • Solid understanding of GMP regulations and quality systems

Job DescriptionActalent is Hiring a Team of Analytical Scientists!!Job Description We are seeking a team of Analytical Chemists to join our team, performing routine tests on various samples, including finished products, stability samples, and raw materials. This role involves using techniques such as UV and HPLC in a regulated laboratory environment, evaluating test results, maintaining accurate documentation, and ensuring compliance with SOPs and cGMP standards. Responsibilities • Conduct routine tests of finished products, stability samples, raw materials, and CV samples using techniques such as assays, chromatographic purity, and particle size distribution., • Evaluate test results and determine the acceptability of samples based on the results., • Maintain accurate lab notebooks and complete all related analytical reports and documentation in compliance with SOPs., • Ensure laboratories are maintained with good housekeeping practices and in compliance with cGMP standards., • Review notebooks promptly and ensure compliance with SOPs., • Analyze and interpret results in both written and oral formats., • Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed., • Follow all SOPs and safety guidelines to ensure compliance with a cGMP environment.Skills & Qualifications, • Bachelor’s degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis, or a Master’s degree with 1 year of experience., • Proficiency in HPLC, UPLC, and UV-Vis techniques., • Familiarity with FDA and GMP regulations., • Ability to analyze and interpret complex data. 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 Hollywood,FL. Application Deadline This position is anticipated to close on Oct 24, 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.

Bachelors degree in Chemist or Science discipline and/or equivalent work experience.

Responsible for routine chemical analysis work and reviewing involving pharmaceutical raw materials, process intermediates and finished products following GMPs.

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Bachelor of Science in Construction Management, Engineering or related discipline.

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Bachelor of Science in Construction Management, Engineering or related discipline.

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Bachelor of Science in Construction Management, Engineering or related discipline.

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