"Attention! Exciting Job Opening at Cipla Pharma - Apply Now!"

Cipla Pharma QC Job Opening – Apply Online

At Cipla Pharma, we strive to provide the highest quality pharmaceutical products to improve the lives of people around the world. We are currently seeking a Team Member_QC to join our Quality department. If you have 1-3 years of experience in the QC department of a pharmaceutical organization and possess strong domain knowledge, we encourage you to apply.

Requisition ID: 81115

Division: Quality

Department: Quality

Employment Type: Permanent

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.


I. Prepare documents

  • 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

II. Review latest pharmacopeial updates

  • 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
  • Escalate non-conformances timely to avoid any delays in operation

III. Review assigned documents

  • Follow the approved procedures and current Cipla policies for review approach by referring valid backup documents, SOPs etc. so that every document is complying w.r.t. the quality aspect of the product
  • Identify and discuss queries / problems faced during the document review by taking initiatives so that further delay in document completion is avoided

IV. Issue documents to applicable units

  • Issue applicable bound books to units by maintaining the log of the same so the current format is available to record the relevant information
  • Maintain correct and updated record of all the issuance of documents and bound books

V. Execute harmonization and simplification process of documents

  • 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

M.Sc. / B. Pharma

Relevant Work Experience

1-3 years of experience in QC department of a pharmaceutical organization


  • Collaborate to Succeed
  • Innovate to Excel
  • Perform with Accountability
  • Lead with Empathy
  • Act with Agility
  • Strong Domain Knowledge
  • People Management

Link to Original Notification to apply

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