FUJIFILM Biotechnologies is building a large biopharmaceutical manufacturing facility and needs to staff it with individuals capable of performing various manufacturing processes, ensuring compliance, and supporting operational startup.
Requirements
- Qualified Experience on unit operation (e.g., Parts Washer, Autoclave Operation, Compounding/Formulation, Filling with Isolator Technology, or Manual/Automated Visual Inspection)
- BioWorks or BTEC Capstone cGMP coursework preferred
Responsibilities
- Leads, executes and documents manufacturing processing steps and/or manufacturing support activities, process monitoring and control
- Performs in-process testing (pH, conductivity, visual inspection)
- Executes validation protocols according to cGMP Standard Operating Procedures (SOPs)
- Performs Operations for all aspects of Drug Product (e.g., Parts Washer, Autoclave, Formulation, Filling, and Visual Inspection)
- Assists the lead with tasks in manufacturing activities
- Assists with the coordination of daily shift activities
Other
- High School Diploma or GED with 4+ years of direct experience in cGMP manufacturing environment
- Associate's Degree + 2 years direct experience in cGMP manufacturing environment
- Bachelor’s Degree, preferably Life Sciences or Engineering
- Equivalent Military training or experience
- This role may require shift work (weekend and potential for nights)
