Pharma Jobs for Freshers at Cipla | Apply Now for the Junior Team Member Position
Looking to build a strong foundation in pharmaceutical quality control? Cipla is hiring a Junior Team Member – QC at its Rangpo, Sikkim facility. This full-time role offers hands-on experience in sampling, analysis, documentation, and stability studies. If you have a degree in Chemistry or Pharmacy and a keen eye for quality, this could be your gateway to an exciting career in pharma.
- Job Title: Junior Team Member – QC
- Location: Rangpo, Sikkim, India
- Req ID: 92005
About The Company
Cipla Limited is one of India’s leading global pharmaceutical companies, renowned for its mission of providing affordable and high-quality medicines across the world. Founded in 1935 and headquartered in Mumbai, Cipla has a strong presence in over 80 countries with a wide portfolio covering respiratory, oncology, cardiovascular, anti-infective, and other therapeutic segments. Known for its pioneering role in making HIV/AIDS treatment accessible, Cipla focuses on innovation, sustainability, and patient-centric healthcare solutions. Through continuous research and manufacturing excellence, the company contributes significantly to improving global health outcomes.
Job Purpose
Perform sampling, execute and document the analysis of raw materials, packing materials, and finished products. Complete stability studies to ensure compliance with quality parameters and meet SRB targets.
Key Responsibilities:
- Analyse assigned samples and perform chromatographic tests using valid procedures and calibrated instruments.
- Conduct analysis for release of raw materials (RM), packing materials (PM), finished products (FP), and water samples.
- Perform stability testing and ensure accuracy and compliance with specifications.
- Review and validate test data, TDS through LIMS before release.
- Follow SOPs and GLP standards to ensure safety and regulatory compliance.
- Document all analysis activities online using approved formats; maintain system integrity and timely updates.
- Maintain lab cleanliness, dispose of analysed samples as per procedures, and perform equipment calibration and qualification.
- Suggest process improvements and contribute to cost-saving initiatives.
- Participate in automation and process enhancement projects.
Major Challenges:
- Delays due to production plan changes or instrument breakdowns.
- Shortages of required materials.
- Solution: Effective coordination, priority planning, and timely escalations.
Key Interactions:
- Daily coordination with Unit Planning, QC, and Stores.
- Collaboration with QA and CDC for specifications and non-conformance management.
- Liaise with service engineers for equipment issues.
Performance Metrics:
- 3–4 FP batches released per day.
- 3–4 RM analyses are conducted daily.
- Stability studies: ~10 per schedule.
- Non-conformance closure: within 7 working days.
Educational Qualification: B.Sc. (Chemistry) or B.Pharm.
Experience: 0–3 years in pharmaceutical QC.
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