Job Location: Vacaville, CA Job Duration: 12 Months Shift: Wednesday – Friday, with alternating Saturdays, 6:00 PM – 7:00 AM (approx. 13-hour shifts) Training Schedule: first 2 weeks Monday – Friday, 8:00 AM – 5:00 PM. Shift Restriction Note: Candidates must be fully available to work the designated day-shift hours during the initial 2-week training period before transitioning to the permanent night shift.
Summary: Responsible for producing innovative bio-therapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment; maintaining areas in high state of inspection preparedness and utilizing business systems for inventory and process management. Maintain records to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Participate in the routine production of mammalian cell culture products within the Vacaville Manufacturing Facility, operating in at least one of the following production areas:
Fosters safe work practices Operate systems that clean and sterilize tanks and filtration systems. Prepare materials for the production process. Exhibit detail-oriented documentation skills to ensure Right-First-Time operations (e.g. tickets, labels, equipment reading) Escalate process issues as necessary to ensure resolution of issue Comply with cGMP, SOP and manufacturing documentation. Use automation to perform production and equipment operations. Provide support to Manufacturing to meet production demands. Assemble and prepare equipment for production. Communicate effectively and professionally in a team environment.
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