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 la...

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