Cipla has announced a new Team Member – QC job opening in Rangpo, Sikkim for candidates with a B.Pharm or M.Sc qualification and relevant pharmaceutical Quality Control experience.
This Cipla QC recruitment 2026 opportunity is suitable for candidates with 1–3 years of experience in the QC department of a pharmaceutical organization who understand regulatory standards, pharmacopoeial requirements, documentation, SOPs, and cGMP compliance.
The selected candidate will primarily work on QC documentation, pharmacopoeial updates, specifications, analytical procedures, document review, harmonization, and compliance activities.
Cipla Team Member QC Job Overview
| Details | Information |
|---|---|
| Company | Cipla |
| Position | Team Member – QC |
| Department | Quality Control |
| Qualification | M.Sc / B.Pharm |
| Experience | 1–3 Years |
| Location | Rangpo, Sikkim |
| Country | India |
| Job Req ID | 105874 |
| Posting Date | 8 August 2026 |
| Industry | Pharmaceutical |
| Job Function | Quality Control / QC Documentation |
About the Cipla QC Role
The primary purpose of the Team Member – QC position at Cipla is to prepare, update, and review specifications, Standard Operating Procedures (SOPs), policies, and operating documents used for material analysis.
The role helps ensure that QC activities remain aligned with predefined quality parameters, applicable pharmacopoeial standards, regulatory requirements, and current Good Manufacturing Practices (cGMP).
Key Responsibilities
1. QC Documentation
The selected candidate will prepare and revise documents such as SOPs, specifications, general analytical methods, and other non-routine QC documentation.
The candidate will coordinate with site Quality Control and Quality Assurance teams to ensure documents are available and compliant with applicable requirements.
2. Pharmacopoeial Updates
A major responsibility of this Cipla Quality Control job is reviewing the latest pharmacopoeial updates, supplements, amendments, and revised monographs.
Responsibilities include:
- Reviewing new and revised pharmacopoeial monographs.
- Monitoring the implementation of pharmacopoeial updates.
- Communicating applicable changes to relevant stakeholders.
- Ensuring activities are completed before applicable effective dates.
- Escalating potential non-conformances or delays.
- Reviewing relevant guidelines and updating documents accordingly.
3. SOP and Document Review
The Team Member – QC will review assigned documents against approved procedures, backup documentation, SOPs, and Cipla quality policies.
The candidate will identify discrepancies or queries during document review and coordinate with the concerned stakeholders to resolve issues without unnecessary delays.
4. Document Issuance & Records
The candidate will support controlled issuance of documents and bound books to applicable units.
Responsibilities include maintaining issuance logs and ensuring that the current approved version of documents and formats is available to relevant teams.
5. Document Harmonization
The candidate will participate in harmonization and simplification of documents across units.
This includes:
- Evaluating documents for standardization.
- Coordinating with cross-functional teams.
- Identifying opportunities to simplify existing processes.
- Supporting standardized procedures across the site.
- Providing suggestions for process improvements.
6. Cross-Functional Coordination
The role requires regular interaction with several functions, including:
- Quality Control (QC)
- Quality Assurance (QA)
- Regulatory Affairs (RA)
- CDC
- Analytical Development Laboratory (ADL)
- Research & Development (R&D)
- IPD
- Other cross-functional teams
Qualification Required
Candidates interested in the Cipla Team Member QC vacancy should have:
Education: M.Sc or B.Pharm
Experience: 1–3 years of relevant experience in the Quality Control department of a pharmaceutical organization.
Candidates should also have knowledge of current regulatory standards and pharmaceutical compliance requirements.
Key Skills for Cipla QC Jobs
Candidates can strengthen their application by highlighting relevant skills such as:
- Pharmaceutical Quality Control
- QC Documentation
- Standard Operating Procedures (SOPs)
- cGMP
- Pharmacopoeial Compliance
- Regulatory Compliance
- Document Review
- Specifications
- Analytical Methods
- Change Implementation
- Quality Documentation
- Cross-Functional Coordination
- Data Review
- Good Documentation Practices (GDP)
Knowledge of pharmacopoeias such as IP, USP, BP and Ph. Eur., where applicable to previous work, can also be relevant for pharmaceutical QC documentation roles.
Who Should Apply?
This opportunity is particularly relevant for B.Pharm and M.Sc candidates with 1–3 years of pharmaceutical QC experience.
Candidates currently working in QC documentation, analytical quality control, SOP management, pharmacopoeial compliance, specifications, or related pharmaceutical quality functions may find the position aligned with their experience.
Freshers should note that the official job description specifically asks for 1–3 years of relevant QC experience.
Why Consider This Opportunity?
The role provides exposure to several important pharmaceutical Quality Control activities, including SOP preparation, document review, pharmacopoeial updates, regulatory compliance, cross-functional coordination, and cGMP documentation.
For candidates building a long-term career in pharmaceutical Quality Control and quality systems, this type of role can strengthen experience in regulated documentation and compliance processes.
How to Apply
