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

6 to 9 Years

Education

Masters in Biotechnology or Biotechnology

Competencies

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

📌 Senior Executive (India)
🏢 LUPIN
📍 India