Fresher Quality Control Jobs at Cipla | BPharm Graduates Apply Now
Cipla, a global leader in the pharmaceutical industry, is seeking a Junior Team Member – QC in Baddi, Himachal Pradesh. This role offers the opportunity to work in a dynamic quality control environment, where you will contribute to ensuring compliance with quality standards, perform critical analysis, and support continuous process improvements if you hold a B.Sc. (Chemistry) or B. Pharm graduate looking to begin or advance their career in pharmaceutical quality control. This is an excellent opportunity.
- Job Position: Junior Team Member – QC
- Location: Baddi, Himachal Pradesh, India
- Job ID: 96391
About the Company
Cipla is a global pharmaceutical leader committed to delivering affordable, high-quality medicines that enhance access to healthcare worldwide. With a legacy of over eight decades, Cipla has been at the forefront of innovation, quality, and patient-centric solutions. Operating in more than 80 countries, the company focuses on therapies for respiratory, antiretroviral, urology, cardiology, oncology, and women’s health. Cipla’s commitment to “Caring for Life” drives its mission to deliver cutting-edge research, robust quality systems, and sustainable healthcare solutions that make a lasting difference.
Job Description:
As a Junior Team Member – QC at Cipla, you will be responsible for performing sampling, executing, and documenting analysis of raw materials, packing materials, finished products, and stability studies. You will ensure compliance with laid-down quality parameters, predefined specifications, and standards to meet site release batch (SRB) targets. The role requires strict adherence to GLP, GMP, and safety norms while maintaining accurate documentation and supporting continuous process improvements.
Key Responsibilities:
- Analyze assigned samples and chromatographic tests using valid procedures and calibrated instruments.
- Perform testing for release of raw materials, packing materials, finished products, water analysis, and process/cleaning validation.
- Execute stability sample analysis without errors according to the schedule and review the results against specifications.
- Document all activities in approved formats and maintain system integrity via CIPDox.
- Ensure laboratory upkeep, disposal of samples, and compliance with GLP standards.
- Participate in operational studies, suggest improvements, and support process automation.
- Collaborate with Unit Planning, QA, Stores, and Service Engineers for smooth operations.
Qualifications:
- Education: B.Sc. (Chemistry) or B.Pharm.
- Experience: 0–3 years in a quality control function within a pharmaceutical organization.
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