This is an intermediate position requiring significant understanding and some independent application and adaptation of existing and new scientific methods and knowledge in accordance with GTP, GLP, GMP, and/or FACT standards. Responsible for independently operating standardized scientific procedures and techniques in a highly regulated environment for clinical cell therapy applications that are moderately complex and/or with oversight. Substantial contributor to the planning, design, execution, and interpretation of process optimization experiments (process development and/or assay development); makes detailed observations, records data, and assesses the processes and results for reliability/efficacy/compliance. Drives the preparation of reports, regulatory submissions, and the drafting of standard operating procedures for novel techniques. May participate in the guidance/mentoring of junior staff.

**Required Education and Experience**
Bachelor’s Degree in an engineering o...