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VOLT is currently partnered with an exciting new start-up focused on the development of the next generation T cell therapies to treat cancer. My client are leading at the forefront of scientific treatments for cancer. Allowing their employees clear progression routes, working with world class leading technologies in a state-of-the-art facility.
Provide a high level of specialist technical and GMP production knowledge to develop and implement improvements/changes to production methods, also to processes in association with tech transfer and validation of equipment,
Must be able to provide problem-solving expertise of closed system cell culture production processes by identifying and implementing procedures.
Must be able to develop, justify and implement strategic decisions to ensure a continuous improvement environment.
Play a vital role in executing QC/analytical assays used for in process control and final release from R&D facility to the GMP Production Facility.
Perform cell therapy manufacture protocols for clinical trials in accordance with GMP regulatory and quality standards (MHRA & FDA).
Completion of GMP batch documentation and ensure their accuracy.
Support continued development and process improvement to further streamline and optimise manufacturing methods.
MSc/BSc degree in life sciences, engineering or related field.
Over 5 years' experience in a GMP environment
2 years of experience in cell therapy, immunology or immunotherapy.
Experience in manufacturing ATMPs complying with MHRA, HTA, FDA.
If you believe you have the necessary skillset to potentially make my shortlist please do reach out via LinkedIn, email or telephone.