Abzena, who provides the most complete set of solutions in integrated early discovery to mid-phase bio-therapeutic and ADC drug development services in the pharmaceutical industry is currently hiring for Quality Control Associate, Stability Coordinator. This role will give you the opportunity to work on a wide range of molecules from companies and academic groups all over the world, including most of the top 20 biopharmaceutical companies.
Summary: The Quality Control Associate will be responsible for performing multiple tasks within the Quality Control (QC) group in support of GMP large-molecule manufacturing activities. This position is expected to oversee and execute stability programs including coordination of internal and external testing for Abzena San Diego projects. Independently defines and executes stability protocol requirements for Abzena San Diego stability testing services. Independently collects, analyzes for trends and generates reports of stability data for Abzena San Diego clients. This position exhibits project coordination skills, the ability to organize and schedule workload to satisfy regulatory and project deadlines as it relates to stability testing, and the ability to effectively convey project status communications to appropriate internal and external customers. The position requires experience within a QC setting and knowledge of GMP/GDP.
Duties and Responsibilities: