Glenmark Pharmaceuticals
Website:
glenmarkpharma.com
Job details:
Qualification - M.Sc / B. Pharm
Experience - 13 - 17 years
Work Location - Haridwar
Job Responsibilities -
- Ensure GMP/GLP compliance at designated Contract Manufacturing sites and third party sites at Haridwar / Roorkee location.
- Ensure availability of current valid master documents like raw material /packing material /finished product specifications, BMR/ BPR at site and retrieval of obsolete documents.
- Review of production plan and execution at sites, ensure BMR, BPR of batches manufactured.
- To check and find non compliance's at Contract Manufacturing /Third Party location and ensure corrective and preventive action.
- To execute, ensure and monitor process validation / Technology Transfer activities, QMS Compliance at site and arrange for the reports.
- To provide registration documents and required support for registration from site.
- Ensure destruction of expired Raw material / primary packing material and Finished product at Contract Manufacturing site.
- Periodic review of control samples at Contract Manufacturing site.
- Preparation and submission of annual product review report for Contract Manufacturing products manufactured at site.
- Review of Third Party product data and COA at site. Compliance verification and Monitor joint analysis at Contract Manufacturing site.
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