Cipla Careers: Junior Team Member QC Job | MSc Chemistry Graduates Apply Now
Are you looking for QC jobs in the pharmaceutical industry with strong compliance exposure? Cipla Careers is offering an excellent opportunity for a Junior Team Member – QC at its Rangpo, Sikkim facility. This role is ideal for professionals seeking MSc Chemistry jobs who want hands-on experience in SOP documentation, pharmacopoeial compliance, and cGMP-driven quality systems.
About Cipla
Cipla is a globally respected pharmaceutical company known for its commitment to quality, innovation, and patient-centric healthcare solutions. Through Cipla Careers, the organization offers a wide range of QC jobs that focus on maintaining high standards of compliance, data integrity, and regulatory excellence across its manufacturing sites.
Cipla’s quality systems are built around robust documentation practices, pharmacopoeial compliance, and continuous improvement. The QC function plays a vital role in supporting regulated operations by ensuring SOP accuracy, timely updates, and adherence to cGMP requirements. Cipla Careers provides a supportive environment for professionals seeking long-term growth, particularly for those pursuing MSc Chemistry jobs in quality control and regulatory documentation. Employees are encouraged to collaborate, improve processes, and contribute meaningfully to the organization’s quality-driven culture.
- Job Title: Junior Team Member – QC
- Location: Rangpo, Sikkim
- Req Id: 99652
Sub Department: 1
Job Purpose: Prepare, update, and review the specifications, SOPs, policies, and operating documents for analysis of materials to ensure alignment with 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 regarding 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 perthe 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 timely 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 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 pharmacopeial updates 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.
