Manufacturing QA Associate (2nd Shift)

The Manufacturing QA Associate contributes to Quality Assurance on the floor activities related to drug substance manufacturing.

• Use fundamental knowledge of GMP, and established procedures methodologies to provide quality oversight of manufacturing documentation, housekeeping, and overall GMP compliance
• Ensure the site performs in a state of compliance by contributing to Quality oversight activities while fostering an empowered culture of quality across all functions
• Execute real time review of batch documentation and other manufacturing documentation analyzing for errors, corrections, and compliance
• Support Transfer Master Cell Banks to Manufacturing
• Perform housekeeping and GMP walkthroughs of facility
• Initiate deviations in real-time and assist in investigations
• Work in cross-functional teams to meet and exceed timelines
• Execute or review room and line clearances
• Make quality decisions in real-time according to regulations ICH Q7 and 21CFR211 and internal procedures
• Support/initiate analytical test results initial investigation on the floor
• Reviews and may approve manufacturing analytical testing on the floor