Job Description

Responsible for ensuring cGMP compliance in the Quality Control Laboratory Responsible for establishment of policies, procedures and practices associated with laboratory activities including safety, testing scheduling and documentation Responsible to ensure the release of In-process, finished products, Raw materials, Packaging Materials Validation Sample and Stability Sample Perform trainings and supervise staff in use of instrumentation and testing techniques, protocols, procedures and ensure all QC documents to be in line with Pharmacopoeia requirements Responsible for OOS and OOT along with risk assessment Responsible for Organizing, ensuring the execution of the Calibration activities, performance verification preventive maintenance and Qualification of QC instruments/equipment’s Ensure Compliance of Analytical Method Validation, Verification and Analytical Method Transfer, API, IPFP, Stability, Excipients, Packing Material Specification, STP’s, ROA’s, RDS, Protocols Reports etc Ensure overall Compliance of Microbiological Laboratory Maintain data integrity and appropriate traceability