QC Manager

Job Title: Quality Control (QC) ManagerIndustry: Nutraceuticals / Dietary Supplements (CDMO)Location: New Brunswick, NJJob SummaryThe Quality Control (QC) Manager is responsible for overseeing all laboratory and quality control functions within a dietary supplement CDMO environment. This role ensures that raw materials, in-process samples, and finished products meet established specifications and comply with regulatory requirements including FDA 21 CFR Part 111 and cGMP standards. The QC Manager will lead laboratory operations, manage a team of analysts, and support timely product release while maintaining the highest standards of quality, safety, and data integrity.ResponsibilitiesOversee testing of raw materials , in – process samples and finished products .Ensure compliance with product specifications and release criteriaReview and approve Certificates of Analysis (COAs)Manage sampling plans, test schedules, and batch release timelinesSupervise day-to-day QC laboratory operations (chemical and microbiological testing)Ensure proper calibration, maintenance, and operation of analytical instruments (HPLC, GC,UV-Vis, etc.)Maintain laboratory SOPs, test methods, and documentationSupport internal, customer, and regulatory auditsMaintain audit readiness and address observationsLead investigations for OOS (Out-of-Specification) and OOT (Out-of-Trend) resultsLead, train, and mentor QC analysts and lab personnelManage team performance, hiring, and developmentPromote a strong quality and compliance culturePartner with QA, Manufacturing, R&D, and Supply Chain teamsSupport product development, scale-up, and tech transfer activitiesDrive improvements in lab efficiency, turnaround time, and cost optimizationQualificationsBachelor’s or Master’s degree in Chemistry, Biochemistry, Microbiology, Food Science, orrelated field5+ years of experience in Quality Control within dietary supplements and nutraceuticals.Experience in a CDMO or contract manufacturing environment preferredHands-on experience with analytical techniques such as HPLC, GC, UV-Vis (ICP-MS is a plus)Strong knowledge of microbiological testing methodsExperience with method validation and stability studiesAbility to work in a fast-paced, multi-client CDMO environmentEffective communication and stakeholder management