Junior Team Member QC Jobs at Cipla
Cipla is hiring a Junior Team Member – QC at its Rangpo, Sikkim location. This Quality Control Job role is an excellent opportunity for B. Pharm graduates to gain hands-on experience in quality documentation, pharmacopoeia compliance, and cGMP standards within a regulated pharmaceutical manufacturing environment. Graduates seeking B Pharma jobs or Pharma Jobs can apply now.
- Job Title: Junior Team Member – QC
- Location: Rangpo, Sikkim, India
About the Company
Cipla is a globally recognized pharmaceutical company committed to quality, compliance, and patient-centric healthcare solutions. Cipla’s manufacturing and quality teams operate under strict regulatory standards, ensuring consistent product quality, robust documentation systems, and continuous improvement across all sites. This Quality Control Job role plays a significant role in the company.
Educational Requirements
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B. Pharm from a recognized institution
Key Responsibilities
- Prepare, update, and review SOPs, specifications, and non-routine QC documents
- Revise corporate analytical documents in coordination with QC and QA teams
- Review pharmacopoeia updates, supplements, amendments, and monographs
- Ensure timely implementation of pharmacopoeia changes to avoid non-conformances
- Maintain online documentation, deviations, and system integrity using approved platforms
- Issue controlled documents and bound books while maintaining accurate issuance records
- Support harmonization and simplification of QC documents across multiple units
- Coordinate with QC, QA, RA, R&D, ADL, and IPD teams for data and document updates
- Escalate documentation gaps, delays, and compliance risks proactively
- Ensure compliance with GMP, GDP, and data integrity requirements
Skills Required
- 1–3 years of experience in QC documentation within a pharmaceutical organization
- Strong understanding of pharmacopoeia standards and cGMP compliance
- Experience in SOP preparation, review, and document control systems
- Ability to manage timelines and work with cross-functional teams
- High attention to detail and documentation accuracy
- Problem-solving approach for handling compliance and process challenges
Why This Job Role?
- Strong entry-to-mid-level QC role at a leading pharma company
- Hands-on exposure to pharmacopoeia updates and regulatory documentation
- Opportunity to work with cross-functional quality and regulatory teams
- Builds a solid foundation for careers in QC, QA, or Regulatory Affairs
- Ideal for B. Pharm professionals aiming to grow in regulated pharma environments
- Graduates seeking B Pharma jobs or Pharma Jobs can apply now.
