Manager
Cadila Pharmaceuticals Ltd
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Posted: 06 Jul 26
Job Description
Lead and maintain the site Quality Management System in compliance with cGMP, ICH, WHO, USFDA, EU GMP, and other applicable regulatory requirements.
Review and approve SOPs, specifications, protocols, reports, and quality documents.
Ensure effective implementation of change control, deviation management, CAPA, risk assessment, and annual product quality review.
Provide QA oversight for API manufacturing operations.
Ensure compliance with Batch Manufacturing Records (BMR), Batch Packaging Records (where applicable), and Good Documentation Practices (GDP).
Review and approve batch records and support batch disposition/release.
Monitor critical manufacturing processes and ensure adherence to validated procedures.
Job Particulars
Role head quality
Education Any Graduate
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id2919556
Job Category Quality Control
Locality Address
State Gujarat
Country India
About Company
Cadila Pharmaceuticals Ltd
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