BPharm/BSc Chem QC Job – at Cipla, Apply Now!
Looking to start your career in pharmaceutical quality control? Join Cipla, one of India’s most respected pharmaceutical companies, as a Junior QC Analyst at their Rangpo, Sikkim facility. This role offers hands-on training in raw material, packaging material, finished product, and stability testing in a world-class GMP environment. Ideal for freshers and early-career professionals in B.Sc. (Chemistry) or B.Pharm streams.
- Job Position: Junior Team Member – QC
- Location: Rangpo, Sikkim, India
- Req Id: 95647
About the Company
Founded in 1935, Cipla is a global pharmaceutical leader known for its commitment to “Caring for Life.” Headquartered in Mumbai, Cipla operates in over 80 countries and is renowned for providing affordable, high-quality medicines in respiratory, antiretroviral, oncology, and critical care. With a legacy of innovation and ethical business practices, Cipla continues to pioneer breakthroughs that make healthcare more accessible and equitable around the world.
BPharm/BSc Chem QC Job Purpose
To conduct timely, accurate analysis of materials and products, perform stability testing, and ensure full documentation and compliance with regulatory quality standards. This role supports Cipla’s mission to ensure safe, effective, and high-quality medications.
BPharm/BSc Chem QC Job – Key Responsibilities
- Perform routine and stability analysis of raw materials (RM), packaging materials (PM), finished products (FP), and water samples.
- Use analytical techniques and instruments such as HPLC, GC, UV, and others as per validated SOPs.
- Enter and maintain data in LIMS, ensuring integrity, traceability, and accuracy.
- Conduct cleaning validation, calibration, and documentation review.
- Follow cGMP, GLP, safety protocols, and maintain lab hygiene.
- Contribute to process automation, troubleshooting, and productivity improvements.
- Coordinate with production, planning, QA, stores, and engineering teams to ensure timely batch release.
BPharm/BSc Chem QC Job – Who Should Apply
- Educatio – n: B.Sc. in Chemistry or B.Pharm
- Experience: 0–3 years in pharmaceutical quality control (freshers encouraged)
- Skills:
- Practical knowledge of lab instruments (HPLC, GC, UV)
- Understanding of GMP, GLP, and documentation standards
- Strong observation, accuracy, and time management skills
- Familiarity with LIMS and analytical software is preferred
Key Interactions & Metrics
- Coordinate daily with Unit Planning, QA, and Stores
- Handle 3–4 RM/PM/FP samples per day
- Complete 10 stability studies per month
- Ensure <1.5% non-conformance and OOS closure within seven working days
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