CQV Biotech Project Lead - GMP Compliance & Commissioning

A leading technical support provider is seeking a qualified individual to develop and maintain commissioning and qualification (C&Q) procedures in Juncos, Puerto Rico. The ideal candidate will have at least 2 years of experience in GMP manufacturing within the biotech or pharmaceutical industry and a relevant degree. Key responsibilities include managing project timelines, collaborating on technical documentation, and ensuring compliance with regulatory standards. This role offers an opportunity to contribute to high-quality standards in life sciences. #J-18808-Ljbffr