Executive
Cadila Pharmaceuticals Ltd
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Applied
Posted: 25 Feb 26
Job Description
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 Particulars
Role head quality
Education Any Graduate
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id2848293
Job Category Quality Control
Locality Address
State Gujarat
Country India
About Company
Cadila Pharmaceuticals Ltd
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