Latest Pharma Job at Cipla | Apply Now for the Team Member Role
Cipla is hiring a Team Member – QMS & Compliance for its site in Rangpo, Sikkim. This Pharma Job requires a B.Pharm or M.Pharm degree and specialized experience in pharmaceutical QA/QMS, particularly within formulations or microbiology. The successful candidate will lead batch documentation reviews, manage CAPAs and deviations, and ensure the site remains in a constant state of audit readiness for DCGI and other health authorities.
- Job Title: Team Member – QMS & Compliance
- Location: Rangpo
- Req Id: 96475
About The Company
Cipla is a global pharmaceutical leader dedicated to ensuring that no patient is denied access to high-quality, affordable medicines. Driven by the “Caring for Life” philosophy, the company operates state-of-the-art manufacturing units across India, including a vital hub in Rangpo, Sikkim. Cipla’s Quality Management Systems are built on the principles of GxP compliance, continuous improvement, and uncompromising data integrity. Joining Cipla means working with a multidisciplinary team to address complex manufacturing challenges while navigating an evolving global regulatory landscape.
Job Purpose
Support the implementation and maintenance of Quality Management Systems (QMS) and compliance activities at the site level. Assist in batch documentation review, deviation handling, CAPA tracking, audit readiness, and regulatory compliance. Ensure timely execution of quality processes and contribute to continuous improvement initiatives.
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.
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.
Key Accountabilities (5/6)
Key Accountabilities (6/6)
- Major Challenges
Ensuring timely and accurate documentation in a fast-paced environment. Maintaining compliance amidst evolving regulatory expectations. Coordinating with cross-functional teams for effective CAPA implementation. Supporting audit readiness with limited prior notice.
Education Qualification
B.Pharm/M. Pharm is required for the Cipla Job
Relevant Work Experience
2–5 years in pharmaceutical QA/QMS roles, preferably in formulations or microbiology.
