Regulatory Site Quality Specialist
Location: hybrid (Florham Park, NJ
Type: Contract | Full-Time
Industry: Large Consumer Packaged Goods (CPG) Company
Job Overview
We are seeking a Regulatory Site Quality Specialist to support a leading CPG company’s OTC drug listing portfolio. This role will manage the drug listing process for skincare and cosmetic products, ensuring compliance with FDA regulations and GMP standards. You will collaborate with cross-functional teams to review and approve change requests, deviations, and CAPAs, while providing GMP consultation and supporting regulatory operations.
Key Responsibilities
Required Skills & Experience
Nice to Have
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