The Scientist I/II will develop and optimize radiochemistry processes for drug production, support CMC activities, and ensure compliance with regulatory standards.

The Associate Director, Quality Systems leads the integration of quality management systems, oversees GMP documentation, collaborates cross-functionally, and manages GxP training programs.

The role involves ensuring compliance with sterility assurance standards, managing Aseptic processes, and supporting quality management in pharmaceutical production.

The Associate Director, MS&T Compliance will lead compliance for manufacturing activities, focusing on investigations, change management, and regulatory alignment in radiopharmaceuticals.

The Quality Control Microbiologist conducts microbiological testing and ensures adherence to quality standards while maintaining laboratory equipment and tracking project timelines.