Job Opportunity
A biopharmaceutical client is seeking a highly skilled professional to manage inspection systems in a sterile drug product facility.
* The ideal candidate will have experience in developing CQV testing documentation and ensuring compliance with GMP guidelines.
This full-time role involves collaborating with cross-functional teams, managing risks associated with inspection systems, and overseeing the development of risk mitigation strategies. The successful candidate should possess excellent communication skills and strong technical knowledge of pharmaceutical manufacturing processes.