On-Site In-Process QA Specialist (GMP)

A global pharmaceutical company located in Sacramento is seeking an In Process QA Specialist to ensure quality standards during manufacturing processes. Key responsibilities include real-time monitoring, testing, and documentation in line with Good Manufacturing Practices. The ideal candidate will have a Bachelor's degree in Life Sciences or related field and up to three years of relevant experience. The position fosters a culture of quality and continuous improvement, offering competitive pay and comprehensive benefits. #J-18808-Ljbffr