Company Information Advent Bioservices is a Contract Development and Manufacturing Organisation (CDMO) providing GMP manufacturing of ATMPs and related products, process development and ancillary services. We support the development of complex, breakthrough therapies for a globally diverse market. We are at the forefront of revolutionary medicine in which life-threatening diseases are treated using highly personalised therapies. Job Summary We are looking for GMP Production Scientists to progress their career with us in the exciting area of cell and gene therapies. As a GMP Production Scientist I or II, you will report to a Production Scientist II, Team Lead or Production manager depending on your role. You will work within the GMP manufacturing team, with responsibility for delivery of cellular therapy products. The GMP Production Scientist will work in a Grade A-D cleanroom environment, ensuring excellent upkeep of the cleanrooms and performing batch manufacturing patient products in biological safety cabinets, isolators. The post holder will work closely with other departments and facilitate the efficient delivery of cellular therapy products for clinical use. This role requires you to work on-site in our Cambridge facility. Responsibilities will include: Working under Good Manufacturing Practice and MHRA regulations Qualifying on Gowning, Transfer of Items and Operator Broth (Operator Aseptic Qualification) to enable you to manufacture cellular products. Cleaning of cleanrooms and equipment. Disinfection of items going into the cleanrooms (Transfer of Items Processes). Performing Environmental Monitoring of cleanrooms. Acting as an Operator, Support or Verifier in manufacturers (dependent on experience/ job seniority). This involves operating and working with cells in an open process inside a Grade A safety cabinet, or Grade B/C cleanrooms in closed system processing. Adhering to a Quality Management System (writing non-conformances, change controls, risk assessments and other GMP documentation). Use of digital platforms such as eBMR and Labware for documenting processes. Use of GMP equipment such as ROTEA, CRF and Liquid Nitrogen Dewars to process / freeze cell therapy products. Line management, supervision and training of staff on processes (Production Scientist II only). You will have the following experience/qualifications: A Bachelor’s degree (or equivalent) in a science or related discipline. A Master’s degree or experience in a cell therapy / pharmaceutical manufacturing environment is advantageous. Experience of cell culture techniques (essential). Experience in aseptic techniques (essential). Experience following validated SOPs and protocols (essential). Working knowledge of GMP for ATMPs and EU regulations for cell and gene therapy (essential). Experience manufacturing in a controlled clean-room environment at Grades A-C (desirable). Experience of writing reports, change controls, and reporting on deviations, non-conformances, and other quality events using a Quality System (desirable). Experience in automation and closed system processing (desirable). Ability to work in a team environment with excellent communication (essential). Ability to adapt to changing environments and to problem solve and make important decisions that affect vital products and services (essential). Candidates must be eligible to work in the UK.