QC Manager
Elite Recruit LLC
East Brunswick, NJ (In Person)
Full-Time
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Job Description
Type:
full-timeJob Description:
Job Title:
Quality Control (QC)Manager Industry:
Nutraceuticals / Dietary Supplements (CDMO)Location:
New Brunswick, NJ Job Summary The 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 includingFDA 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. Responsibilities Oversee testing of raw materials , in - process samples and finished products . Ensure compliance with product specifications and release criteria Review and approve Certificates of Analysis (COAs) Manage sampling plans, test schedules, and batch release timelines Supervise 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 documentation Support internal, customer, and regulatory audits Maintain audit readiness and address observations Lead investigations for OOS (Out-of-Specification) and OOT (Out-of-Trend) results Lead, train, and mentor QC analysts and lab personnel Manage team performance, hiring, and development Promote a strong quality and compliance culture Partner with QA, Manufacturing, R D, and Supply Chain teams Support product development, scale-up, and tech transfer activities Drive improvements in lab efficiency, turnaround time, and cost optimization Qualifications Bachelor's or Master's degree in Chemistry, Biochemistry, Microbiology, Food Science, or related field 5+ years of experience in Quality Control within dietary supplements and nutraceuticals. Experience in a CDMO or contract manufacturing environment preferred Hands-on experience with analytical techniques such as HPLC, GC, UV-Vis (ICP-MS is a plus) Strong knowledge of microbiological testing methods Experience with method validation and stability studies Ability to work in a fast-paced, multi-client CDMO environment Effective communication and stakeholder managementSimilar remote jobs
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