Senior OfficerJobs Opening in Cadila Pharmaceuticals Ltd at Ankleshwar
FEATURED JOBSenior Officer
Cadila Pharmaceuticals Ltd
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Posted: 09 Jul 26
Job Description
Monitor shop floor activities to ensure compliance with cGMP, SOPs, approved Batch Manufacturing Records (BMR), and regulatory requirements.
Review Batch Manufacturing Records (BMR), logbooks, equipment records, and GMP documentation for accuracy and completeness.
Perform line clearance, area clearance, equipment clearance, and in-process verification before and during manufacturing activities.
Review and investigate deviations, incidents, OOS, OOT, market complaints, and implement effective CAPA.
Coordinate Change Control, Quality Risk Management (QRM), and quality improvement initiatives.
Support process validation, cleaning validation, equipment qualification, and utility qualification activities.
Review and approve SOPs, protocols, reports, specifications, and validation documents.
Ensure compliance with Data Integrity (ALCOA+), Good Documentation Practices (GDP), and electronic record requirements.
Conduct internal GMP audits, self-inspections, and support customer and regulatory inspections (USFDA, MHRA, EU GMP, WHO GMP, TGA).
Monitor environmental conditions and GMP compliance across production and warehouse areas.
Coordinate with Production, QC, Engineering, Warehouse, and EHS to resolve quality and compliance issues.
Mentor and guide QA Officers and junior team members on GMP and quality systems.
Maintain QA metrics, compliance reports, and trend analysis for management review.
Job Particulars
Role head quality
Education Any Graduate
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id2921245
Job Category Quality Control
Locality Address
State Gujarat
Country India
About Company
Cadila Pharmaceuticals Ltd
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