CQV QA Specialist: GMP Validation & Compliance

A global biotech company is looking for a Quality Assurance Specialist - CQV to ensure compliance and oversight in pharmaceutical manufacturing environments. Key responsibilities include reviewing CQV documentation, ensuring GMP compliance, and providing guidance during system design. The ideal candidate will have a Bachelor’s degree and 4-7 years of experience in a GMP-regulated environment. This position offers a competitive salary and benefits, and aims to deliver on commitments to customers. #J-18808-Ljbffr