Responsibilities Review and approve production and analytical documentation accompanying the release of drug substance, drug product and packaged finished goods to ensure conformance to appropriate SOPs, GMP and regulatory requirements, including supporting QP certification.
Perform and review complaints and deviation investigations, change controls and CAPAs. Creates and maintains assigned SOPs. Compile data for reports and presentations, provides data interpretation draws conclusions. […]
Actively communicate and collaborate with functional areas to develop a strong working relationship and understanding...