QC Jobs at Cipla | MSc Chemistry Graduates Apply
QC Jobs at Cipla. They are inviting applications for the role of Junior Team Member – QC at its Baddi facility in Himachal Pradesh, MSc Chemistry Jobs.. This opportunity is ideal for M.Sc. Chemistry and B.Pharm graduates eager to advance in the field of pharmaceutical quality control. The role involves preparing and reviewing SOPs, specifications, and analytical documents to ensure compliance with pharmacopeial standards and cGMP guidelines. Apply for the MSc Chemistry Jobs.
- Job Title: Junior Team Member – QC
- Posting Date: 26 Oct 2025
- Country: India
- State: Himachal Pradesh
- Location: Baddi
- Req Id: 98188
Job Purpose:
Prepare, update, and review the specifications, SOPs, policy, and operating documents for analysis of materials in order to ensure alignment to predefined quality parameters and compliance with respective standards/pharmacopeia 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 with respect to operating documents.
Key Accountabilities (2/6):
- Review the latest pharmacopoeial updates, supplements, and amendments by evaluating the updates required in the available document to ensure compliance with the current pharmacopoeia through consent with the regulatory body.
- 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 concerned stakeholders to initiate and complete activities before the effective date of the pharmacopoeia.
- 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 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 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 correct and updated records 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 simplify work.
Key Accountabilities (6/6):
Major Challenges:
- Delay in verifying methods for pharmacopeial updates due to data unavailability. Overcome by coordinating with QC and.
- Insufficient time was allotted to update the documents due to late notifications and shifting priorities. Overcome by understanding the requirements and proper planning, and coordination with CFTs.
- There is a delay in meeting the final timelines for activities due to delayed review comments from cross-functional departments. Overcome by regular follow-ups and escalations.
Key Interactions (1/2):
- CDC/QC/QA/RA to obtain approval for documents (Daily).
- ADL/R&D to obtain data for document updates for the 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 updates upon receipt of supporting data.
Dimensions (2/2):
Key Decisions (1/2):
- Process simplification and modification to other locations, CDC / Section Head – CDC.
- Resolution of user queries to the Section Head – CDC.
Key Decisions (2/2):
Education Qualification:
M.Sc. / B. Pharma.
Relevant Work Experience:
1-3 years of experience in the QC department of a pharmaceutical organization with knowledge of the latest regulatory standards and compliance norms.
