CQV Specialist — Upstream & Downstream Biotech Equipment

A leading technical solutions provider is seeking a CQV Specialist to develop and validate protocols for biotech process equipment. The ideal candidate has a Bachelor’s degree in a relevant field and 3–5 years of experience in qualification and validation activities. Strong knowledge of GMP and FDA regulations along with excellent communication and teamwork skills are essential. This role operates in a dynamic environment where you will collaborate across functions to ensure compliance with industry standards. #J-18808-Ljbffr