Senior QA Lead, GCP​/PVG Compliance & Audit Strategy

A leading global pharmaceutical company in New Jersey is seeking an Associate Director of Quality Assurance-GCP/PVG. This role entails overseeing GCP compliance for clinical trials, managing quality assurance audits, and ensuring adherence to regulatory standards. Ideal candidates will have over 10 years of pharmaceutical experience, a solid GCP auditing background, and the ability to lead teams effectively. Excellent communication skills and a proactive mindset are essential.

The position offers the opportunity to lead quality initiatives and collaborate with multiple departments to ensure compliance.
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