The purpose of the role is to ensure the day-to-day execution of GMP manufacturing operations at Adaptimmune Manufacturing suite. Working closely with a team of manufacturing specialists, the focus of the role is to deliver GMP batches of viral vector for Adaptimmune clinical programme. Responsibilities include operating bioprocessing equipment, executing routine cleanroom maintenance and supporting environmental monitoring. The role will also require on the job training in aseptic operations and writing and reviewing GMP documentation.
The role is based at the Cell and Gene Therapy Catapult Manufacturing Centre, Stevenage, UK.
Qualifications & Experience
Skills & Competencies
Decision Making Authority
The job holder is responsible for reporting and escalating any non-compliance and operational deviations to the team lead. The job holder will alternate the roles of “main operator” or “verifier” for the purpose of batch record completion. The job holder is expected to take part to weekly team rota as per manufacturing schedule.
Additional “on-call” responsibilities may be taken on a voluntary basis.
In order to enter the clean room environment the following things need to be taken into consideration: