Deputy Manager
DholkaFull-timeMid levelPosted over a month ago
Mid-level pharma role at Cadila Pharmaceuticals in Dholka.
About the role
Planning and execution of Validation, Qualification, Re-Qualification and Re-Validation activities pertaining to Manufacturing facility at Dholka site in line with the cGMP requirements of national and international regulatory authorities. To Perform Vendor Management Activity to assure that Vendors are Complying with Cadila SOP on Vendor Management and GMP Requirements in Order to source Quality Materials and Products.
What you'll do
- Perform the validation exercises of new as well as existing equipment’s, utilities and critical systems
- Prepare and update Annual Validation Master Planner and Equipment Matrix of all Blocks
- Prepare, review, execute and compile the protocol and report of Transportation Validation
- Prepare, review protocol and reports and execute activity related to Aseptic Process Simulation (Media fill) Studies
- Perform the in process checks for control on production for the process / product being manufactured
What you need
- GMP
- SOP writing
- HVAC
- Reconciliation