Chemist

Job Title: Technical Manufacturing ChemistJob Description The Technical Manufacturing Chemist supports an infectious disease diagnostics business by producing high-quality materials used in immunology-based chromatography and enzyme tests. This role focuses on preparing critical and non-critical bioreagents, performing in-process quality control testing, and maintaining robust quality and safety standards in a regulated manufacturing environment. The chemist collaborates closely with a production team to meet scheduled output while continuously improving processes and supporting product performance. Responsibilities Maintain and support the established production schedule by planning and executing daily manufacturing activities on time. Produce material for use in immunology-based chromatography and enzyme tests according to defined procedures and quality standards. Prepare critical and non-critical bioreagents for use in products and manufacturing processes by following detailed Standard Operating Procedures (SOPs). Perform in-process quality control (QC) testing of manufacturing materials, including qualification checks, quality inspections, and titration, to ensure products meet specifications. Investigate problem areas in the manufacturing process, identify root causes, and propose or implement improvements to enhance quality, efficiency, and consistency. Identify and explore areas of desirable process improvement and contribute to continuous improvement initiatives. Create, follow, and refine protocols designed to improve products and manufacturing processes, ensuring documentation is accurate and up to date. Maintain quality systems and adhere to Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) requirements in all activities. Undertake new procedures and methods as needed, ensuring proper safety precautions are always observed and documented. Use laboratory instruments such as pipettes, spectrophotometers, HPLC systems, pH meters, and gel electrophoresis equipment to support manufacturing and testing activities. Perform ELISA and related assays as part of product and process characterization and quality control. Work collaboratively in a team setting, coordinating manufacturing efforts based on the production schedule and communicating effectively with colleagues. Monitor and maintain the supply of raw bioreagents to support ongoing production requirements, escalating issues when supply risks arise. Use computer applications, including spreadsheet, database, manufacturing, and word processing software, to document work, record data, and support production planning. Work both independently and as part of a team with moderate supervision, managing priorities and ensuring assigned tasks are completed accurately and on time. Essential Skills Bachelor's degree in Chemistry, Life Sciences, or a related field, or an equivalent combination of education and experience. Hands-on experience using pipettes for accurate liquid handling in a laboratory or manufacturing environment. Experience with spectrophotometry for quantitative analysis of samples. Experience operating High-Performance Liquid Chromatography (HPLC) systems. Experience using pH meters for solution preparation and control. Experience performing gel electrophoresis for analysis of biomolecules. Experience with SDS-PAGE techniques for protein analysis. Experience performing ELISA assays for qualitative or quantitative analysis. Ability to work successfully as a member of a team and independently with moderate supervision. Proficiency using computer applications, including spreadsheet, database, manufacturing, and word processing software. Strong attention to detail and adherence to Standard Operating Procedures (SOPs). Ability to follow and maintain Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) standards. Additional Skills & Qualifications Experience in immunology-based chromatography or enzyme test manufacturing. Familiarity with in-process QC testing, including qualification, inspection, and titration methods. Experience working within a regulated diagnostics or life sciences manufacturing environment. Demonstrated ability to contribute to process or product improvement initiatives. Strong documentation skills for recording protocols, test results, and production data. Comfort working with new procedures and adapting to evolving processes and technologies. Work Environment This role operates in a laboratory-based manufacturing environment within an infectious disease diagnostics business unit. The chemist works with immunology-based chromatography and enzyme test materials and regularly uses laboratory equipment such as pipettes, spectrophotometers, HPLC systems, pH meters, and gel electrophoresis apparatus. Work follows a structured production schedule, requiring coordination with a broader manufacturing team and adherence to Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) standards. The environment emphasizes safety, proper handling of reagents and biological materials, and strict compliance with Standard Operating Procedures (SOPs). Work typically involves standard laboratory and production hours, with tasks performed at the bench and in production areas, using computer systems for data entry, documentation, and production planning. Job Type & Location This is a Contract position based out of Scarborough, ME. Pay and Benefits The pay range for this position is $28.00 - $30.00/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 Scarborough,ME. Application Deadline This position is anticipated to close on Jun 23, 2026. 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. 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 process due to a disability, please email View email address on click.appcast.io for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. 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