Manager - Quality Control

About this role

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Skills you'll use

What you'll do

• LIMS Master data review
• 1. Ensure analysis of Semi Finish Product, Stability samples, In Process and Blend Samples and related documentation as per cGMP requirement.
• 2. Ensure entry of data in SAP and release of semi-finished products in SAP.
• 3. Plan the Analysis of Finish Product and stability samples as per cGMP requirement in time.
• 4. Allocation of work as per the skills of persons and supervision.
• 5. Review and approve OOS, OOT and Incident of QC laboratory and carry out OOS investigation.
• 6. To review and ensure effective implementation of regulatory requirement, guidelines and pharmacopeia changes like IP, BP, USP, Ph. Eur, JP etc.
• 7. Review of work output and pending work.
• 8. To perform self-audit of QC Laboratory on periodic basis.
• 9. Ensure analysis of Raw Materials / Finished Products as per requirement from Outside Commercial Lab.

Who can apply

• 5. Review and approve OOS, OOT and Incident of QC laboratory and carry out OOS investigation.
• 6. To review and ensure effective implementation of regulatory requirement, guidelines and pharmacopeia changes like IP, BP, USP, Ph. Eur, JP etc.
• 7. Review of work output and pending work.
• 8. To perform self-audit of QC Laboratory on periodic basis.
• 9. Ensure analysis of Raw Materials / Finished Products as per requirement from Outside Commercial Lab.
• 10. To check audit trail in QC Instruments.
• 11. Ensure compliance to KRA’s and other such assignments.
• 12. To control and maintain QC Laboratory Records. (Like Laboratory note Book, Chromatograms, and COA etc.).
• 13. On job training as necessary to develop skills and improve productivity.
• 14. To ensure cGMP in quality Control laboratory.

About Piramal Pharma

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