Keeps up-to-date on regulations/ development of biopharmaceutical QC method/ technology to ensure the project maximizes the use of digitalization, automation and robotics.
Analyze quality data, implement corrective and preventive actions (CAPA), and continuously improve QA/QC systems, processes, and documentation to enhance operational performance and product quality.
Maintain quality documentation, inspection records, and compliance reports while coordinating with Production, Engineering, and Supply Chain teams on quality-related matters.
Interpret drawings and instructions from operations sheets and complex blueprints, engine manuals, inspection records, and inspection record method sheets