Quality Control Jobs at Cipla | Chemistry Candidates Apply Now
Quality Control Jobs at Cipla. A career as a Junior Team Member in Quality Control offers a strong foundation for professionals aiming to grow in pharmaceutical quality systems, documentation, and regulatory compliance. This role focuses on preparing, reviewing, and updating critical QC documents to ensure alignment with pharmacopeial standards, cGMP requirements, and site-wide quality processes. With responsibilities spanning SOP development, document harmonization, deviation recording, and cross-functional coordination, the position provides an excellent opportunity to build expertise in modern QC documentation and pharmaceutical compliance frameworks. Interested candidates apply or the exciting opportunity at Cipla Careers.
Cipla, a global pharmaceutical company, is dedicated to improving healthcare delivery by developing and producing high-quality, accessible medications. We prioritize innovation and excellence in every aspect of our operations. Join our team and be part of a thriving community where you can make a significant impact.
- Job Title: Junior Team Member – QC
- Posting Date: 5 Dec 2025
- Country: India
- State: Himachal Pradesh
- Location: Baddi
- Req Id: 98185
Department
Sub Department
Job Purpose
Prepare, update, and review the specifications, SOPs, policy, and
Key Accountabilities
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 against the operating documents.
Key Accountabilities
Review the latest pharmacopoeial updates, supplements, and amendments by evaluating the updates required in the available document to ensure compliance with the current pharmacopoeia and obtain regulatory approval.
- Review the new/revised monograph as per the current pharmacopoeia.
- Review the latest pharmacopeial updates and monitor their 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 promptly to avoid any delays in operation.
Key Accountabilities
Document all activities performed as per valid procedures online by using standard/approved formats or templates to ensure that all entries done are correct, accurate, and authentic.
- 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 requirement.
Key Accountabilities
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 the log of the same so the current format is available to record the relevant data entries.
- Maintain the correct and updated record of all the issuance of documents and bound books.
Key Accountabilities
Execute harmonization and simplification of the 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
Major Challenges
Delay in verification of methods for pharmacopeial updates due to non-availability of data. Overcome by coordinating with QC and inadequate time allotted for updating the documents due to late intimations and change in priorities. Overcome by understanding the requirements and proper planning and coordination with CFTs. Delay in meeting final timelines of the activities due to delay in getting review comments for cross-functional departments. Overcome by regular follow-ups and escalations.
Key Interactions
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
Dimensions
Number of units supported for documents update: 4
Average number of documentation (preparation/review) per month: 10
Achieve finalization of NLT 80% documents within defined timeline
Ensure 100% implementation of pharmacopeial updation after getting supporting data
Dimensions
Key Decisions
Process simplification and modification to other locations CDC / Section Head – CDC
Resolution of user queries to Section Head – CDC
Key Decisions
Education Qualification
M.Sc. / B. Pharma.
Relevant Work Experience
1-3 years of experience in QC department of a pharmaceutical organization with knowledge of latest regulatory standards and compliance norms.
