Quality Control is seeking an Associate QC Analyst to support routine analytical and microbiological testing in a GMP-regulated environment. This role is ideal for candidates who are detail-oriented, thrive in fast‑paced settings, and enjoy hands-on laboratory work. You will perform analytical testing, maintain GMP/GDP-compliant documentation, operate laboratory equipment, and ensure adherence to quality and safety standards. Key Responsibilities + Perform a variety of analytical and microbiology-based assays, including: + Titer, MMV, Mycoplasma, Endotoxin, Bioburden, TOC, Conductivity + Centralized Raw Material testing + Compendial testing + Environmental Monitoring + Critical Utilities monitoring + Sample receipt, handling, and aliquoting + Ensure all facilities, equipment, procedures, and products comply with cGMP, GDP, and safety regulations. + Generate accurate, complete, and compliant laboratory documentation in electronic systems and lab notebooks. + Operate laboratory instruments and equipment following established protocols. + Perform review and approval of assays, documents, and laboratory records. + Support investigations, troubleshooting, and problem-solving activities. + Communicate quality, compliance, supply, or safety risks to management promptly. + Support TRAs, deviations, and other quality events as needed. + Complete all required training to maintain qualifications for assigned tasks. + Perform additional duties as assigned by management. What We’re Looking For + Experience performing analytical laboratory tests with strong accuracy, efficiency, and attention to detail. + Ability to work independently and deliver right‑first‑time results. + Strong written and verbal communication skills. + High regard for data integrity and compliance. + Ability to work a 40‑hour workweek (4 x 10‑hour shifts). + Must be legally authorized to work in the U.S. without employer sponsorship. Required Qualifications Candidates must meet one of the following: + Bachelor’s degree in a science-related field + OR + Associate degree and 1–2 years of Quality or Analytical Lab experience + OR + High school diploma/GED and 3 years of Quality or Analytical Lab experience Preferred Qualifications + 1–3 years of experience in a GMP analytical laboratory + Experience executing analytical or biological testing per methods and/or compendial standards + Experience with QC analytical systems and/or quality management systems + Strong organizational skills and ability to manage multiple tasks with minimal supervision + Understanding of GMP, QC laboratory principles, and data integrity requirements + Familiarity with biopharmaceutical processes and related unit operations + Strong analytical skills: ability to collect, organize, analyze, and communicate data with accuracy and clarity + Self-motivated, detail-oriented, and effective in time-sensitive environments + Experience with investigations, deviations, and QC processes Job Type & Location This is a Contract position based out of West Greenwich, RI. Pay and Benefits The pay range for this position is $25.00 - $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 West Greenwich,RI. Application Deadline This position is anticipated to close on Feb 5, 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 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 actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.