OTC Regulatory Quality Lead - GMP & Compliance
Insight Global
A prominent staffing firm is seeking a Regulatory Site Quality Specialist in Florham Park, NJ. The role involves managing the OTC drug listing portfolio, participating in regulatory tasks, and collaborating across teams. Key qualifications include a BS degree in science or engineering and at least 5 years of experience in a GMP environment. Candidates should possess a strong understanding of FDA procedures and be detail-oriented. This is a unique opportunity to work within a dynamic and challenging sector. #J-18808-Ljbffr
Vacancy posted 2 days ago
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