Cipla, one of India’s leading pharmaceutical companies, has announced an exciting opportunity for the position of Junior Team Member – Quality Control (QC). This role is ideal for candidates with a background in pharmaceutical sciences who want to build a strong career in quality assurance and regulatory compliance.
The position is based in Rangpo, Sikkim, and offers hands-on exposure to SOP preparation, documentation management, and compliance with global pharmacopeial standards.
Job Overview
Key Details
- Company: Cipla
- Role: Junior Team Member – QC
- Location: Rangpo, Sikkim, India
- Department: Quality Control
- Experience: 1–3 Years
- Qualification: M.Sc / B.Pharm
- Job Type: Full-time
Job Purpose
The primary purpose of this role is to prepare, review, and update SOPs, specifications, and analytical documents. The candidate will ensure compliance with cGMP requirements and pharmacopeial standards while supporting QC operations.
Roles & Responsibilities
Documentation & SOP Management
- Prepare and revise SOPs, specifications, and analytical methods
- Ensure timely availability of documents for QC analysis
- Coordinate with QC/QA teams for corporate document updates
Compliance & Pharmacopeia Updates
- Review pharmacopeial updates, supplements, and amendments
- Update documentation as per current regulatory standards
- Ensure timely implementation to avoid non-conformances
Data & Documentation Handling
- Maintain accurate documentation using approved formats
- Update systems like CipDox with correct entries and records
- Ensure data integrity and compliance with GMP requirements
Document Issuance & Record Keeping
- Issue documents and maintain issuance logs
- Ensure availability of updated formats across departments
- Track and manage document versions effectively
Process Improvement
- Participate in document harmonization and simplification
- Suggest improvements for standardization across units
- Collaborate with cross-functional teams (CFTs)
Required Qualifications
Educational Qualification
- M.Sc (Chemistry / Analytical Chemistry)
- B.Pharm
Experience
- 1–3 years in QC department of a pharmaceutical company
- Knowledge of regulatory standards and compliance norms
Salary & Benefits
- Estimated Salary: ₹2.8 LPA – ₹5.5 LPA
- Performance-based increments
- Health and insurance benefits
- Career growth in a reputed pharmaceutical organization
- Exposure to regulatory compliance and global standards
Key Skills Required
- Strong knowledge of GMP and pharmacopeia
- Documentation and SOP writing skills
- Analytical thinking and attention to detail
- Team coordination and communication
How to Apply
Interested candidates can apply through Cipla’s official careers portal using the reference ID 101581. Ensure your resume highlights QC experience, SOP handling, and regulatory knowledge.
Why Join Cipla?
Cipla is known for its innovation, compliance excellence, and employee-friendly culture. This opportunity allows you to work on real-time quality systems, collaborate with experienced professionals, and grow in the pharmaceutical industry.