Job Description

Job Description
Division
Department
Sub Department 1
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 / 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 pharmacopeial updates, supplements and amendments by evaluating the updates required in the available document to ensure the compliance with the current pharmac...

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