QC Jobs at Cipla | Chemistry Candidates | Apply Now
Are you looking for QC Jobs in a leading pharmaceutical company that offers growth, learning, and long-term stability? Cipla Careers brings an excellent opportunity for M.Sc. and B.Pharma professionals to join as a Junior Team Member – QC at its Baddi facility in Himachal Pradesh. This role is ideal for candidates with 1–3 years of experience who want to build a strong foundation in quality control, documentation, and regulatory compliance while working with one of India’s most trusted pharma brands.
About Cipla:
Cipla is one of India’s most respected pharmaceutical companies with a strong global presence across over 80 countries. Known for its commitment to quality, innovation, and patient-centric healthcare, Cipla Careers offers excellent opportunities for professionals seeking long-term growth. Working in QC Jobs at Cipla provides hands-on exposure to world-class quality systems, regulatory standards, and continuous learning, making Cipla Jobs a preferred choice for pharma professionals across India.
- Country: India
- State: Himachal Pradesh
- Location: Baddi
- Req Id: 100018
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 w.r.t 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 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 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.
- 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 from 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 documents update: 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.
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.
