Analytical Lab Manager

POSITION SUMMARY:

The Analytical Laboratory Manager is responsible for overseeing Quality Control.

Laboratory operations supporting cosmetic and OTC drug products. This role ensures all analytical testing, method validation, stability programs and data integrity practices comply with FDA regulations, cGMPs, USP requirements, and internal quality standards. The position manages laboratory personnel, equipment, and investigations while supporting product release and regulatory readiness.

• Manage day-to-day operations of the QC analytical laboratory for raw materials, in-process, finished goods, and stability samples.
• Ensure timely and compliant testing to support batch release for cosmetic and OTC drug products.
• Establish and maintain laboratory procedures, test methods and specifications.

• With Quality Assurance/Regulatory guidance, ensure laboratory compliance with:
• 21 CFR 210/211 (OTC drugs)
• 21 CFR 700 (cosmetics)
• USP/NF, ISO 22716 and internal SOPs
• Support FDA inspections, audits and regulatory inquiries.
• Initiate laboratory investigations, OOS, deviations and CAPAs.

• Oversee method validation, verification and transfer for chemical and physical tests (e.g. assay, impurities, ph, viscosity, preservative content)
• Maintain analytical method lifecycle documentation.

• Manage stability programs for OTC products, including protocol generation, data review and expiry dating support.
• Support shelf life extensions with scientific justification where applicable.

• Ensure qualification, calibration and maintenance of laboratory instruments (HPLC, UPLC, GC, UV-Vis, balances, etc.)
• Oversee laboratory systems (Access databases and SYSPRO - ERP)
• Ensure proper handling of reference standards and reagents.

• Supervise, train and mentor QC analysts and technicians.
• Ensure staff are trained in cGMPs, safety and laboratory procedures.
• Conduct performance reviews and support professional development.

• Review and approve laboratory notebooks, worksheets, electronic data, and reports.
• Participate in SOP authoring and periodic review.

Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences or related field.

• 5-8+ years experience in QC analytical testing within cosmetics, OTC drugs or pharmaceuticals.
• 2+ years in a supervisory or managerial laboratory role.
• Direct experience with FDA inspections and regulatory audits.

• Strong knowledge of USP methods, OTC monographs, and cosmetic testing requirements.
• Hands-on experience with chromatographic and spectroscopic techniques.
• Experience with stability studies, OOS investigations and method validation.