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Hobson Prior is seeking a QCVM to join a leading biotechnology organization contract basis. In this role, you will be responsible for overseeing the qualification and transition of analytical procedures for genetic therapy materials and products, ensuring adherence to EU and FDA GMP regulations. This role entails overseeing the end-to-end management of analytical procedures, laboratory instruments, and associated materials across dual locations in the UK and Ireland.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities: Lead the development and validation of testing methods for gene therapy products. Act as the go-to expert for managing analytical methods, equipment, and materials. Create and maintain documentation to support analytical activities while meeting compliance standards. Ensure all testing methods meet regulatory and data integrity requirements. Oversee external testing activities to ensure they comply with GMP standards. Manage projects to implement new testing methods within set timelines. Train team members on new technologies and methodologies introduced to the facility. Regularly assess and improve analytical methods to ensure optimal performance.

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