Job Description

Job Description

Work Base Location - Puducherry

Operating locations - Puducherry, Chennai & Hyderabad

Educational Qualification - M. Pharm / M. Sc

Experience - 04 - 07 years quality working experience in OSD / Gels / MDI (Sterile formulation)

Job Responsibilities -

  • Ensure GMP/GLP compliance at Contract Manufacturing sites and third party sites and provide registration documents and required support for registration from site.
  • - Review of batch manufacturing record /batch packing record and clearance for batch release.
  • - To check and find non compliances 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.
  • - Ensure destruction of expired Raw material / primary packaging material and finished product at CMO.
  • Periodic review of control samples at Contract Manufacturing sites.
  • Review of annual product review report for products manufactured at Contract Manufacturing sites.
  • Verification of RM/PM testing as per GPL specification & Sampling Plan at Contract Manufacturing /Third Party Site and approval of site master documents.


Job Details

Role Level: Mid-Level Work Type: Full-Time
Country: India City: Nashik ,Maharashtra
Company Website: http://www.glenmarkpharma.com Job Function: Management
Company Industry/
Sector:
Consumer Services And Pharmaceutical Manufacturing

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