QC Jobs in Pharma: Cipla is Hiring a Junior Team Member in Sikkim | Apply Now for Cipla Career
Looking for QC jobs in Pharma? Join as a Junior Team Member – QC in Rangpo, Sikkim, and play a key role in preparing, updating, and reviewing critical quality documents and SOPs. This role ensures compliance with regulatory standards, pharmacopeia, and cGMP guidelines, offering a great opportunity for those seeking Cipla career.
Job Details:
- Job Position: Junior Team Member – QC
- Location: Rangpo, Sikkim, India
- Req ID: 96520
About the Company:
Cipla is a global pharmaceutical company headquartered in India, renowned for its commitment to affordable, high-quality medicines and innovative healthcare solutions. With a presence in over 80 countries, Cipla focuses on patient-centric care, research, and development, producing medicines for chronic and acute conditions across multiple therapeutic areas.
The company thrives on a culture of innovation, quality, and compliance, guided by cGMP standards. Cipla emphasizes employee development, continuous learning, and process excellence, empowering its workforce to contribute to improving global healthcare access and outcomes.
Education & Experience:
- Qualification: M.Sc. / B.Pharm.
- Experience: 1–3 years in a QC department of a pharmaceutical organization with sound knowledge of regulatory standards and compliance norms.
Key Accountabilities:
1. Document Preparation & Review
- Prepare documents like SOPs, specifications, and non-routine documentation to ensure timely availability across the site.
- Revise corporate documents like SOPs and analytical methods by coordinating with site QC/QA.
- Review applicable pharmacopoeia and update documents accordingly.
- Check instrument calibration data in line with operating documents.
2. Compliance & Updates
- Review latest pharmacopeial updates and implement necessary revisions for compliance.
- Evaluate new or revised monographs per current pharmacopeia.
- Ensure timely implementation of updates to avoid non-conformances.
- Communicate and escalate non-conformances as required.
3. Documentation & Data Integrity
- Record all activities as per valid procedures using approved templates.
- Maintain documentation integrity and update records on CipDox.
- Prepare and revise documents as per GMP requirements.
4. Document Issuance & Record Keeping
- Issue documents to units and maintain issuance records.
- Keep logs of all issued bound books to ensure the current version is always available.
- Maintain accurate and updated issuance records.
5. Process Simplification & Standardization
- Execute document harmonization and simplification to standardize procedures.
- Coordinate with cross-functional teams (CFTs) for document alignment.
- Provide suggestions for process improvement and work simplification.
Major Challenges & Solutions:
- Delayed verification of methods: Addressed by coordination with QC teams.
- Limited time for updates: Managed through better planning and prioritization.
- Review delays: Minimized through regular follow-ups and timely escalation.
Key Interactions:
- Internal: CDC, QC, QA, RA (daily communication).
- Cross-functional: ADL, R&D, IPD (as needed for data and updates).
Performance Dimensions:
- Support 4 units for document updates.
- Prepare or review an average of 10 documents per month.
- Achieve finalization of ≥80% documents within the defined timeline.
- Ensure 100% implementation of pharmacopoeial updates post data validation.
Key Decisions:
- Process simplification and modification under guidance from Section Head – CDC.
- Resolve user queries and ensure documentation consistency across locations.
