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Quality Control Specialist

Telix Pharmaceuticals Limited
August 30, 2026
Full-time
Remote friendly (Angleton, TX)
Worldwide
Operations
Role: QC Specialist supporting GMP manufacturing of radiopharmaceuticals, focusing on analytical and biological testing to ensure product quality and compliance. Responsibilities: execute QC tests (HPLC, GC, TLC, Elisa, CE-SDS) on radioactive materials, review data for batch release, perform method validation, investigations (OOS, deviations), and maintain GMP standards; support regulatory interactions and laboratory management activities. Requirements: Bachelor's in chemistry, biochemistry, biology, or related field; 3+ years in GMP lab environment; experience with QC techniques, GxP operations, and aseptic procedures preferred; ability to work with radioactive materials and follow safety protocols. HighValue: radiopharmaceuticals, GMP, QC testing, radioactive materials, GxP manufacturing, regulatory support, biologics and small molecules. WorkSetup: hybrid or remote; collaboration across functions is required.