Technical Assistant Job in CPL Pharmaceuticals Private Limited at Udaipur

"1. To perform the validation exercises of new as well as existing equipment's, utilities and critical systems. 2. Preparation, Execution, Compilation & Review of qualification and Validation Protocols & Reports. 3. Preparation, Review, approval & authorization of SOP. 4. To prepare and update Annual Validation Master Planner and Equipment Matrix of all Blocks. 5. Line clearance activity, review and approval of batch manufacturing and packing record and compile the protocol and report of Transportation and process Validation. 6. Coordination with cross functional teams for smooth conduction of validation activities with respect to: Equipment, HVAC and various Qualification/Re-Qualification, Validation/Re-Validation Batch record review and approval. FG release, PR, PO and other activities in SAP and Artwork review and approval. 7. To initiate and review change control, deviation and CAPA. 8. To prepare, review protocol and reports and execute activity related to Aseptic Process Simulation (Media fill) Studies 9. Responsible to assist for handing of activities related to Vendor Approval. 10. To Perform Vendor Audits for Vendor Qualification as per requirement of RM/PM. 11. To assist for preparation of Approve Vendor List of RM/PM and to assist for preparing Vendor Grading of RM/PM based on Rejection of Supply from Vendors on Yearly Basis. Any other jobs assigned from time to time."