This job is with Autolus Therapeutics, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ business community. Please do not contact the recruiter directly. Role Summary The MSAT Associate plays a key role in supporting manufacturing operations, process improvements, and technical troubleshooting for Autolus’ cell therapy products. This position provides hands-on support in technology transfer, process validation, and continuous improvement initiatives to ensure the robustness and scalability of manufacturing processes. The MSAT Associate collaborates closely with cross-functional teams, including Manufacturing, Quality, Process Development, and others, to maintain compliance with GMP standards and drive operational excellence. Key Responsibilities Input, manage and analyze process performance data to identify trends and optimize manufacturing operations. Provide technical support to GMP manufacturing operations (including shopfloor presence), troubleshooting process-related issues and driving continuous improvement initiatives. Ensure up to date with relevant and required training applicable to job role. Work along side manufacturing schedule Support technology transfer activities, including the transfer of processes from development to GMP manufacturing and between sites. Assist in the execution of process validation, including data analysis and documentation. Participate in process risk assessments and implement mitigation strategies to enhance process robustness. Collaborate with Process Development to assess process scalability and define critical process parameters. Author, review, and revise technical documents, including standard operating procedures (SOPs), batch records, protocols, and reports. Support investigations, out-of-specification/trend (OOX), root cause analysis for deviations and non-conformances and contribution towards corrective/ preventive actions (CAPAs). Assist in the evaluation and implementation of new technologies to enhance manufacturing efficiency and product quality. Maintain compliance with GMP regulations, company policies, and industry best practices. Author/ review/ approve raw material specifications used within commercial manufacture Demonstrated skills and competencies Bachelor’s or Master’s degree in Biotechnology, Biochemical Engineering, Life Sciences, or a related field. Experience in a GMP-regulated biopharmaceutical or cell therapy manufacturing environment is preferred. Knowledge of cell therapy manufacturing processes, including aseptic techniques, bioreactors, and cryopreservation, is a plus. Strong analytical and problem-solving skills with the ability to interpret complex data sets. Excellent communication and collaboration skills to work effectively in a cross-functional team. Ability to work in a fast-paced, dynamic environment with attention to detail and adherence to deadlines. Familiarity with regulatory requirements, including MHRA, FDA, and EU GMP guidelines, is desirable. LI-DNI