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Piramal Pharma Ltd

Senior Executive-QA

Piramal Pharma Ltd Kohir mandal, Telangana, India

Pharmaceutical Manufacturing · 1,001-5,000 employees

Oct 21
qa Senior (5-10 yrs) Full-time India
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About the role

The Senior Executive-QA is responsible for reviewing analytical data, audit trails, and system compliance within the Quality Control department. They ensure that all intermediates, finished products, and stability batches meet quality standards before release.

What they look for

Quality Assurance Analytical Data Review Audit Trail Review Chromatographic Instruments Non-chromatographic Instruments SOP Compliance Laboratory System Compliance Quality Control Data Invalidation Contamination Control Stability Data Analysis IPC Data Review

Requirements

The candidate must hold a Master of Science (MSc) degree. They are expected to have experience in laboratory system compliance, SOP adherence, and the identification of potential contamination risks.

Full description

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Division

Piramal Pharma SolutionsPiramal Pharma Solutions is a contract development and manufacturing  organization (CDMO), offering end-to-end development and manufacturing  solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.  

This enables us to offer a comprehensive range of services including Drug Discovery  Solutions, Process & Pharmaceutical Development services, Clinical Trial  Supplies, Commercial supply of APIs and Finished dosage forms. We also offer  specialized services like development and manufacture of Highly Potent APIs  and Antibody Drug Conjugation.  

Our capability as an integrated service provider  & experience with various technologies enables us to serve Innovator and  Generic companies worldwide.  

For more details, please visit : www.piramalpharmasolutions.com

Job Title

Senior Executive-QAJob Description

Review of Audit trails of the Chromatographic instruments and Non chromatographic instruments. Daily review and release of analytical data of intermediates, finished products, stability data and IPC data• Responsible for the review of In-process analytical data before release.

  • Responsible for the review of Intermediates, stability batches and Finished products before release.
  • Responsible for the release of Intermediates and finished products.
  • Responsible for the review of System audit trails of the instruments in QC.
  • Verification of various logbooks for completeness in QC area.
  • Responsible for the invalidation of the analytical data.
  • Identify and report the potential areas of contamination/Cross contamination.
  • Verifying the SOP’s compliance in shop floor.
  • Carry out the audits as and when required for laboratory system compliances.
  • Report any incident/accident/near miss to the superiors.

Master of Science (MSc)

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