Senior Scientist

Shift: Wednesday - Saturday

Location: Irvine, CA

• Support the BI Lab in managing day-to-day operations related to manufacturing, materials, facilities, scheduling, engineering, and maintenance to ensure smooth, continuous, cost-effective, and controlled production
• Plan, prepare, issue, and control production schedules and material requirements to ensure timely availability of approved materials aligned with production forecasts and inventory goals
• Serve as shift or operational lead as required to maintain production execution, area readiness, and GMP compliance

• Perform hands-on production and testing activities as needed to support execution, training, troubleshooting, or elevated business demand
• Apply scientific techniques to culture and test spores used in the biological indicator manufacturing process
• Prepare, review, and technically assess batch records in accordance with cGDP

• Lead and support complex product deviations, process excursions, and production issues using scientific, technical, and statistical diagnostic methods
• Apply standard scientific principles, theories, and concepts to evaluate process performance and implement corrective and preventive actions
• Provide developmental and technical support for both new and existing products

• Identify opportunities to improve existing processes, systems, and equipment to increase efficiency, improve quality, and reduce cost
• Design, execute, and interpret experiments to optimize manufacturing processes and reduce variability
• Lead or co‑lead Kaizens and other continuous improvement initiatives
• Monitor process performance metrics and ensure sustained improvements through data-driven decision making

• Bachelor’s Degree in Biology, Microbiology, Biochemistry, Chemical Engineering, or a related scientific discipline required
• Master’s Degree preferred
• 4–8+ years of experience in a regulated biologics or medical device manufacturing environment
• Demonstrated experience leading technical projects, investigations, or cross‑functional initiatives
• Experience with process development, process improvement, and operational support in manufacturing environments

• Advanced knowledge of cGMP and cGDP requirements
• Strong experience working in FDA‑regulated environments and Medical Device manufacturing
• Expertise in aseptic processing and biologics manufacturing
• Ability to design experiments, analyze data, and interpret results
• Strong written and verbal communication skills
• Proficiency with Excel and data analysis tools
• Preferred Qualifications:
• Knowledge of SAP inventory management systems
• Experience with statistical tools (e.g., Minitab)
• Yellow Belt or Green Belt certification (Black Belt a plus)
• Train‑the‑Trainer or Training Within Industry (TWI) experience
• Knowledge of process control systems and automation

• Domestic travel up to approximately 10%
• On‑call or weekend support may be required
• Ability to lift 31–50 lbs
• Ability to wear required PPE
• Ability to work in a manufacturing laboratory environment

This position is also eligible for bonus as part of the total compensation package.

The salary range for this position (in local currency) is 101,.

Fortive Corporation and all Fortive Companies are proud to be equal opportunity employers. We value and encourage diversity and solicit applications from all qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity or expression, or other characteristics protected by law. Fortive and all Fortive Companies are also committed to providing reasonable accommodations for applicants with disabilities.