QA Operations Lead - Global GMP, Batch Release (Hybrid)
Telix Pharmaceuticals Limited
A leading radiopharmaceutical company in Angleton seeks a QA Operations Specialist to manage quality-related activities and ensure regulatory compliance at the manufacturing site. Candidates should have a relevant bachelor's degree and at least 3 years of experience in quality assurance. Responsibilities include overseeing manufacturing quality, supporting regulatory interactions, and maintaining cGMP standards. This dynamic role offers competitive compensation and a focus on improving patient lives through innovation in medicine. #J-18808-Ljbffr
Vacancy posted 4 days ago
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