“QC Junior Team Member Opportunity: Apply Now with B.Pharm/MSc at Cipla”


Website Cipla

About Cipla

Cipla Limited is a global pharmaceutical company based in Mumbai, India. It was founded in 1935 by Dr. K.A. Hamied, and today it is one of the largest pharmaceutical companies in India and a significant player in the global pharmaceutical industry.

Cipla is known for its focus on providing affordable and accessible healthcare solutions. The company is involved in the development, manufacturing, and marketing of a wide range of pharmaceutical and healthcare products, including prescription drugs, active pharmaceutical ingredients (APIs), and over-the-counter (OTC) medications.

Cipla has a diverse portfolio that covers various therapeutic areas, such as respiratory, anti-infectives, cardiovascular, central nervous system, gastro-intestinal, oncology, and more. The company has a strong presence in both domestic and international markets, with a significant footprint in over 80 countries.

In addition to its pharmaceutical business, Cipla is actively involved in research and development, striving to bring innovative and cost-effective solutions to address global health challenges. The company has played a crucial role in providing affordable medicines for various diseases, including HIV/AIDS, tuberculosis, and malaria.

Post: Junior Team Member – QC

Job Description:

Job Purpose: Prepare, update, and review specifications, Standard Operating Procedures (SOPs), policies, and operating documents for material analysis. Ensure alignment with predefined quality parameters and compliance with relevant standards, pharmacopeia, and current Good Manufacturing Practice (cGMP) requirements.


I. Document Preparation:

  • Prepare documents like SOPs, specifications, and non-routine documentation.
  • Ensure timely availability across the site to provide support during the analysis.

II. Pharmacopeial Compliance:

  • Review the latest pharmacopeial updates, supplements, and amendments.
  • Evaluate updates required in the available document to ensure compliance with current pharmacopoeia through consent with regulatory bodies.

III. Quality Compliance:

  • Review assigned documents by referring to the relevant backup and pre-defined quality procedures.
  • Ensure compliance against quality requirements.

IV. Document Issuance:

  • Issue documents to applicable units.
  • Maintain a record in the issuance record (bound book) to ensure the current version of the common document is available at the unit.

V. Harmonization and Simplification:

  • Execute harmonization and simplification processes of documents.
  • Reduce complexities in processes and ensure standardized procedures are followed.

Candidate Profile:

  • Educational Qualification: M.Sc. / B.Pharma
  • Experience: 2 years in the QC department of a pharmaceutical organization


  • Collaborate to Succeed
  • Innovate to Excel
  • Perform with Accountability
  • Lead with Empathy
  • Act with Agility
  • Strong Domain Knowledge
  • People Management

Additional Information:

  • Experience: 2 years
  • Qualification: M.Sc. / B.Pharma
  • Location: Sikkim – Rangpo
  • Industry Type: Pharma/ Healthcare/ Clinical Research
  • End Date: 30th March 2024

This opportunity is ideal for candidates with a strong background in Quality Control, holding an M.Sc. or B.Pharma degree, and possessing 2 years of relevant experience. If you are a dynamic professional who thrives in a collaborative environment and has a passion for maintaining high-quality standards in pharmaceuticals, we invite you to apply. The position is based in Sikkim – Rangpo, and the application deadline is 30th March 2024. Join us in contributing to the healthcare and clinical research industry with innovation, accountability, and excellence.

To apply for this job please visit career10.successfactors.com.