Cipla, as an organisation has been built brick-by-brick on the foundation of care. Caring For Life has always been and continues to remain, our guiding purpose. Driven by the same purpose, we have extended our presence to 80+ countries providing over 1,500 products across various therapeutic categories in 50+ dosage forms. To make healthcare more affordable globally, we are deepening our presence in the key markets of India, South Africa, the U.S. among other economies of the emerging world.
Post : Team Member - QMS & Compliance
Job Description
Key Accountabilities (1/6)
Batch Documentation Review
Review batch manufacturing records and ensure completeness and compliance with SOPs
Deviation and CAPA Support
Assist in documentation and tracking of deviations, change controls, and CAPAs. Participate in root cause analysis and follow-up actions
Audit and Inspection Readiness
Maintain audit trail documentation and support audit preparation activities. Ensure timely closure of audit observations
Key Accountabilities (2/6)
QMS Documentation
Maintain and update QMS-related documents such as SOPs, APQRs, and quality agreements.
Training and Compliance Monitoring
Participate in GxP training programs and monitor adherence to compliance standards.
Regulatory Support
Assist in implementing DCGI notifications and other regulatory updates
Key Accountabilities (3/6)
Risk Assessment Participation
Support risk assessment exercises and contribute to mitigation planning
Product Evaluation and Recall Coordination
Assist in product evaluation activities and support recall coordination under supervision.
Batch Documentation Review
Review batch manufacturing records and ensure completeness and compliance with SOPs.
Key Accountabilities (4/6)
Deviation and CAPA Support
Assist in documentation and tracking of deviations, change controls, and CAPAs. Participate in root cause analysis and follow-up actions
Audit and Inspection Readiness
Maintain audit trail documentation and support audit preparation activities. Ensure timely closure of audit observations
QMS Documentation
Maintain and update QMS-related documents such as SOPs, APQRs, and quality agreements.
Training and Compliance Monitoring
Participate in GxP training programs and monitor adherence to compliance standards
Candidate Profile
B.Pharm / M.Pharm
2–5 years in pharmaceutical QA/QMS roles, preferably in formulations or microbiology
Additional Information
Experience : 2–5 years
Qualification : B.Pharm / M.Pharm
Location : Rangpo - Sikkim
Industry Type : Pharma/ Healthcare/ Clinical research
End Date : 28th February 2026
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