Learn and execute Cell Therapy Manufacturing operations Perform patient process unit operations and complies with operations described in standard operating procedures and batch records Executes transactions and process in all electronic systems Prioritizes safety of self and others Reports safety events within 24 hours Escalates any/all issues that may impact safety of self and/or others. Complete documentation required by governing controlled documents and batch records Perform all tasks in a manner consistent with the safety policies, SOPs, quality systems, and GMP requirements Complete training assignments to ensure necessary technical skills and knowledge Train for proficiency in process systems and some supporting business systems Execute the daily unit operations schedule, that includes people, product, and material flow across multiple shifts Maintain manufacturing environmental conditions (Non-Viable Particulate(s) and Viable microbial levels per controlled area classification specifications) by performing area disinfection regiment as required to meet global Health Authority requirements Continues to refine and improve manufacturing process technique to improve individual operational times. Ensures training completion prior to production Work in areas that may have strong magnets Work in areas with exposure to vapor phase liquid nitrogen Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Associate or bachelor's degree in related field is preferred A minimum high school diploma and/or equivalent combination of education and experience is required 0-1 years of cGMP cell therapy manufacturing, bioprocessing manufacturing, or relevant experience and education Proven experience working on teams where collaboration and results were expected Proficiency in common computer tools such as word processing, spreadsheet and web-based applications Meticulous attention to detail and personal accountability is critical to success Possess excellent interpersonal skills, is attentive and approachable Maintain a professional and productive relationship with area management and co-workers Basic understanding of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing is preferred
