Sterile Process Validation Lead

5 days ago


Oxford, Oxfordshire, United Kingdom Oxford Biomedica Full time
Job Overview

We are seeking a Sterile Process Validation Lead to join our team at Oxford Biomedica. In this role, you will be responsible for validating sterile processes and ensuring compliance with GMP regulations.

About the Role

This is an exciting opportunity to contribute to the maintenance of overall department KPIs relating to validation of equipment, facilities, utilities, processes, and computerised systems. You will work closely with the Validation Department to ensure that all manufacturing processes meet industry guidelines.

Key Responsibilities
  • Validation of sterile processes
  • Maintenance of KPIs
  • Supporting technology transfer activities
Requirements
  • A Degree in a Science or Engineering discipline
  • Working knowledge of current standards, GMP regulations, and industry guidelines
  • Demonstrable experience of validation of manufacturing processes in a biopharmaceutical industry
  • Experience of working within a GMP Quality Management System


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