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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 Senior Research Associate I/II will conduct LC-MS-based bioanalysis for pharmacokinetics, proteomics, and ADME studies, performing sample preparation and method execution.