Job Description

Job Description

  • Visiting to DS manufacturing and warehouse facility to ensure that activities are being carried out by following GMP requirements, Regulatory requirement and as per approved procedures.
  • To participate in the manufacturing investigation and CAPA finalization activity.
  • Preparation and review the Risk Assessment and Mitigation Plan.
  • Ensure that process and cleaning validation activities are being carried out by following approved protocols.
  • Review of master document like study protocol, BPR, MFR etc.
  • Review of executed Batch Processing Records for Batch Release.
  • Review of Batch Dispatch Record and verification of dispatch activities in warehouse.
  • Overall coordination for the APQR data compilation and APQR preparation activity.
  • Preparation and review of Quality System SOPs & documents.
  • Review of SOPs as per GMP requirements for all departments.

Work Experience

3 to 5 years.

Education

Masters in Biotechnology

Post Graduation in Pharmacy or Pharmaceutical Technology

Competencies

  • Innovation & Creativity
  • Customer Centricity
  • Developing Talent
  • Result Orientation


Job Details

Role Level: Not Applicable Work Type: Full-Time
Country: India City: Pune/Pimpri-Chinchwad Area
Company Website: http://www.lupin.com Job Function: Quality Assurance & Control
Company Industry/
Sector:
Other

What We Offer


About the Company

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