Onsite QA Specialist: GMP, Audits & Improvement

A leading pharmaceutical company is seeking a Quality Assurance Specialist for their Cidra, PR site. This fully onsite role involves supporting quality systems, leading investigations, and ensuring compliance with regulations. The ideal candidate will have a Bachelor's degree and a minimum of three years of experience in a Quality department within a manufacturing setting. Join a dedicated team committed to improving patient lives and fostering an inclusive environment. #J-18808-Ljbffr