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Katalyst CRO in Vacaville is seeking to produce innovative bio-therapeutic medicines by interfacing with highly automated production systems in a cGMP environment. You will participate in routine production of mammalian cell culture products, operating in upstream and downstream areas, while maintaining inspection readiness and strict SOP compliance.
The role requires attention to detail, ability to work with hazardous materials, and effective teamwork in a rigorous manufacturing setting.
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: