Piramal Pharma Limited
Location
Dhar | India
Job description
Experience:
5-9 Year Experience in Quality Control Chemical and Instrumentation Analysis for In-process, Stability, Raw Materials, Working standard/Reference standard, Packing Materials, intermediates and finished products to meet the dispatch timeline as per the monthly schedule received from PPIC (API) as per Pharma Manufacturing GMP requirements.
Qualification : B.Sc (Chemistry) / M.Sc (Chemistry) / B. Pharmacy / M. Pharmacy
Key Roles & Responsibilities
1. Responsible for the review of In-process analytical data before release.
2. Responsible for the review of Intermediates, stability batches and Finished products before release.
3. Responsible for the release of Intermediates and Semi finished products.
4. Responsible for the review of System audit trails of the instruments in QC.
5. Verification of various log books for completeness in QC area.
6. Responsible for the invalidation of the analytical data.
7. Identify and report the potential areas of contamination/Cross contamination.
8. Verifying the SOPs compliance in shop floor.
9. Carry out the audits as and when required for laboratory system compliances.
10. Report any incident / accident / near miss to the superiors.
11. Identify unsafe conditions and unsafe acts and report to superiors.
12. Any other job as may be assigned to you from time to time by the superior
13. Responsible for the work of his senior in the absence of senior.
14. Comply with SHE guideline, SHE rules and regulations, use the PPE wherever applicable.
Job tags
Salary
