Cadila Pharma

Job responsibility
•	To ensure cGMP compliance at shop floor during manufacturing of vaccines and bio similar.
•	Preparation, Execution and compilation of validation activities pertaining to:
•	Qualification (IQ, OQ and PQ) of new equipments and Utilities (such as Water System, HVAC System, Pure Steam, Compressed Air).
•	Periodic re-qualification of existing equipments and critical systems.
•	Area Qualification.
•	Coordination with External service provider for Execution of Qualification activity.
•	Coordination for execution of CAPA plan/risk mitigation plan, shutdown and to ensure implementation of corrective and preventive action related to qualification activity 
•	Execution and compilation of reports of planner pertaining to qualification/validation and calibration / preventive maintenance activities as per established schedule.
•	Maintain qualification document with proper filing and retrieval of same as and when.
•	Preparation of Purchase Indent.
•	To initiate change control and prepare documents related to qualification activity.
•	To prepare and follow Annual validation Planner.
•	Preparation/revision of  SOP’s related to Qualification & Validation and validation master plan 
•	Report any non-conformance to In-charge/ HOD /Designee if any."

Job Details

Skills Required

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