Clinical Cell Processing Associate

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...