Quality Control Job at Cipla | BPharm Graduates Apply Now for the Junior Team Member Role
A pharmaceutical company in Baddi, Himachal Pradesh, is seeking a Junior Team Member – QC to manage critical documentation and compliance within its Quality Control department. This Quality Control Job is ideal for M.Sc. / B. Pharma graduates with 1-3 years of experience and deep knowledge of regulatory standards. The primary focus is preparing, reviewing, and updating specifications, SOPs, and policy documents while ensuring 100% timely implementation of all pharmacopeial updates to maintain adherence to cGMP requirements and support efficient material analysis across all site units.
- Job Title: Junior Team Member – QC
- Location: Baddi, Himachal Pradesh, India
- Req Id: 98185
About The Company
Since the company name was not provided, this overview is tailored to the job description’s context. The hiring organization is a pharmaceutical company with multi-unit operations, likely a Contract Development and Manufacturing Organization (CDMO) or a large-scale manufacturer, based in Baddi, Himachal Pradesh. The company places critical emphasis on Quality Control (QC) documentation, compliance, and regulatory adherence. Its quality system involves rigorous management of specifications, SOPs, and pharmacopeial updates across multiple units, requiring strong cross-functional coordination (with CDC, QC, QA, and RA) to ensure continuous cGMP compliance and system integrity.
Cipla 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 to respective standards/pharmacopoeia 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 pharmacopeial updates, supplements and amendments by evaluating the updates required in the available document to ensure the compliance with the current pharmacopoeia through consent with regulatory body. Review the new/revised monograph as per current pharmacopoeia. Review the latest pharmacopeial updates and monitor its timely implementation to avoid any non-conformances. Intimate the concerned stakeholders to initiate and complete activities before effective date of 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 done are correct, accurate and authentic. Maintain system integrity by updating documentations 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 (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 the log of the same so the current format is available to record the relevant data entries. Maintain correct and updated record of all the issuance of documents and bound books.
Key Accountabilities (5/6)
Execute 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.
Education Qualification for the Cipla Job
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.
