Job Description

Job Description

  • Co-ordination and communication on routinely basis with US team.
  • Updation of required status and database for Operations, Packaging, MST/ Technical Services .
  • To work in collaboration with team members to create the highest quality documents and timely delivery of outputs consistently.
  • Prepare and review PPQP, PPQR, PSP, PSR, CPVP, BBHS, regulatory modules (for submission/validation batches).
  • Prepare and review Cleaning Validation documents (Matrix, CVP, CVSR & CVR’s) in addition to timely monitoring of Annual Cleaning Verification Program, LOTC, DEHT & CEHT.
  • Handling of CC, UD, PD, Event and Customer complaints as and when required.
  • To prepare and review documents for manufacturing activities which includes but not limited to MPR, PBR, MPS, SOP and other manufacturing related documents.
  • Prepares technical assessment reports and deviations investigations, etc.

Qualifications

B.Sc./ B.Pharm/ M.Sc./ M.Pharm


Job Details

Role Level: Mid-Level Work Type: Full-Time
Country: India City: Ahmedabad ,Gujarat
Company Website: http://www.amneal.com Job Function: Information Technology (IT)
Company Industry/
Sector:
Pharmaceutical Manufacturing

What We Offer


About the Company

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