Responsible for producing innovative bio-therapeutic medicine by interfacing with highly automated production systems and controls in a cGMP manufacturing environment. This role involves maintaining areas in a high state of inspection preparedness and utilizing business systems for inventory and process management. The technician will maintain records to comply with regulatory requirements using current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). The position involves routine production of mammalian cell culture products within the Vacaville Manufacturing Facility, operating in at least one of the following production areas: Upstream Manufacturing (UM) or Downstream Manufacturing (DM). Responsibilities include following established safety and environmental guidelines, immediately reporting safety and environmental incidents, and fostering safe work practices.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED