Cipla Careers: Quality Control Jobs | MSc Chemistry Graduates Apply Now
Are you looking for Quality Control Jobs in the pharmaceutical industry? This Junior Team Member – QC opportunity at Cipla Jobs in Rangpo, Sikkim, is ideal for professionals seeking growth through Cipla Careers. The role focuses on QC documentation, pharmacopeial compliance, and cGMP systems, offering strong exposure for candidates building long-term careers in pharmaceutical quality control and regulatory operations.
About Cipla
Cipla is a globally recognized pharmaceutical company committed to quality, innovation, and patient-centric healthcare solutions. With a strong presence across regulated markets, Cipla Careers offers diverse opportunities in Quality Control Jobs, manufacturing, research, and regulatory functions. Cipla fosters a culture of compliance, learning, and continuous improvement, enabling employees to grow professionally while contributing to global healthcare. Through advanced systems, ethical practices, and a people-first approach, Cipla Jobs provide long-term career stability, skill development, and exposure to world-class pharmaceutical operations.
- Job Title: Junior Team Member – QC
- Location: Sikkim, Rangpo
- Req Id: 96046
Job Purpose
Prepare, update, and review specifications, SOPs, policies, and operating documents for the analysis of materials to ensure alignment with predefined quality parameters and compliance with respective standards/pharmacopeias and cGMP requirements.
Key Accountabilities (1/6)
- Prepare documents like SOPs, specifications, and non-routine documentation, and ensure timely availability across the site to provide support during the analysis.
- Prepare/revise corporate documents like SOPs, general analytical methods, etc., by coordinating with site QC/QA.
- Review the applicable pharmacopoeia and guidelines and make appropriate updates.
- Review instrument calibration data w.r.t operating documents.
Key Accountabilities (2/6)
- Review the latest pharmacopoeial updates, supplements, and amendments by evaluating the updates required to ensure compliance with the current pharmacopoeia through consent with the regulatory body.
- Review the new/revised monograph as per the current pharmacopoeia.
- Monitor its timely implementation to avoid any non-conformances.
- Inform the relevant stakeholders to initiate and complete activities before the pharmacopoeia’s effective date.
- Escalate non-conformances in a timely manner to avoid any delays in operation.
Key Accountabilities (3/6)
- Document all activities performed as per valid procedure online by using standard/approved formats or templates.
- Maintain system integrity by updating documentation and deviations on CipDox while performing operations.
- Maintain all the online documentation and timely entries, and supporting documents.
- Prepare new documents and update existing documents as per GMP requirements.
Key Accountabilities (4/6)
- Issue documents to applicable units by maintaining the record of the same in the issuance record (bound book), so the current version of the common document is available at the unit.
- Issue applicable bound books to units by maintaining a log of the same, so the current format is available to record the relevant data entries.
- Maintain a correct and updated record of all the issuance of documents and bound books.
Key Accountabilities (5/6)
- Execute the harmonization and simplification process of documents to reduce complexities in processes and ensure standardized procedures are followed.
- Evaluate and prepare documents for standardization across all units at a site.
- Coordinate with CFTs and check requirements as per existing procedures to simplify the process.
- Provide suggestions and ideas by exploring new possibilities to achieve work simplification.
Key Accountabilities (6/6)
Major Challenges
- Delay in verification of methods for pharmacopeial updates due to the non-availability of data. Overcome by coordinating with QC and.
- Inadequate time was allotted for updating the documents due to late notifications and changes in priorities. Overcome by understanding the requirements and proper planning, and coordination with CFTs.
- Delay in meeting the final timelines of the activities due to the delay in getting review comments for cross-functional departments. Overcome by regular follow-ups and escalations.
Key Interactions (1/2)
- CDC / QC / QA / RA to get approval on documents (Daily).
- ADL / R&D to get data for document updates for deficiency response (Need Basis).
- IPD to get data for document updates for new projects (Need Basis).
Key Interactions (2/2)
Dimensions (1/2)
- Number of units supported for document updates: 4.
- Average number of documentation (preparation/review) per month: 10.
- Achieve finalization of NLT 80% documents within the defined timeline.
- Ensure 100% implementation of pharmacopoeial updation after getting supporting data.
Dimensions (2/2)
Key Decisions (1/2)
- Process simplification and modification to other locations, CDC / Section Head – CDC.
- Resolution of user queries tothe Section Head – CDC.
Key Decisions (2/2)
Education Qualification: M.Sc. / B. Pharma.
Experience: 1-3 years of experience in the QC department of a pharmaceutical organization with knowledge of the latest regulatory standards and compliance norms.
