GMP-Ready QA/RA Director — Quality & Regulatory Strategy (Raleigh)
Summary
ProPharma is seeking a QA/RA Director to lead GMP readiness and quality system development for a biotech and pharmaceutical ecosystem. The role involves managing QMS, ensuring regulatory compliance, and overseeing vendor qualification in a cross-functional environment.
ProPharma in Raleigh seeks an experienced leader in quality, regulatory, and GxP to guide GMP readiness for a biotech/pharma ecosystem, including instrument, software, and consumables. Lead QMS development, Part 11 adherence, vendor qualification, and cross-functional execution with a lean, scalable approach. The role requires 10 years in life sciences quality/regulatory, and a proven track record building quality systems from the ground up to support GMP projects and customer partnerships. J-1…