×
Register Here to Apply for Jobs or Post Jobs. X

Principal Scientist

Job in Thousand Oaks, Ventura County, California, 91362, USA
Listing for: Fujifilm Corporation
Full Time position
Listed on 2026-07-26
Job specializations:
  • Engineering
    Process Engineer, Validation Engineer
Salary/Wage Range or Industry Benchmark: 150000 - 210000 USD Yearly USD 150000.00 210000.00 YEAR
Job Description & How to Apply Below

Overview

At FUJIFILM Biotechnologies California, we’re driving the future of medicine with the expertise to produce life-changing cell therapies like T-cell and CAR T immunotherapies. Working with pioneering biotech partners, our teams manufacture innovative treatments that improve lives. Join us at our advanced Thousand Oaks facility, where you’ll make a tangible impact on groundbreaking therapies. We offer a collaborative, flexible workplace and a vibrant culture driven by passion and energy—what we call Genki.

If you’re ready to reimagine the future of healthcare, let’s create something extraordinary together. Our campus is in Thousand Oaks, California, an exceptional place to live with great schools, natural beauty, outdoor activities, and proximity to Los Angeles and Santa Barbara. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging.

We are guided and united by our Group Purpose of giving our world more smiles.

Primary Responsibilities
  • Provide strong scientific leadership and hands‑on support for all aspects of technology transfer, process development and scale‑up, lab‑scale process monitoring, and process troubleshooting, and support regulatory submissions as needed.
  • Optimize cell culture and processing methodologies, cell selection and separation technologies, cell characterization methods, and process equipment selection to meet cGMP, Quality Systems, and regulatory requirements.
  • Identify and qualify critical or custom reagents and disposable consumables required for development activities.
  • Design and execute process development studies to develop a thorough understanding of operating and performance parameters (Design space). Implement science‑based approaches and cGMP requirements in the selection of critical raw materials and components.
  • Provide Process Sciences assessments on suitability of technologies, scalability, and manufacturability during process development activities and partner with Process Engineering and clients to define the critical process parameters of new processes.
  • Provide significant technical depth to support troubleshooting efforts during development activities.
  • Assess suitability of technologies, equipment, and methodologies to provide a competitive advantage for our service offering and the efficiency and effectiveness of client programs.
  • Provide leadership in process development assessments for potential clients.
  • Partner with cross‑functional teams such as the Cell Therapy Business leaders, Process Engineering, Technology Transfer/New Product Introduction to ensure successful development and transfer into the site of all client cell therapy manufacturing processes.
  • Develop study templates that can serve as platforms for multiple cell types or processing modules, as applicable.
  • Author, review, and approve process development reports, process qualification protocols and reports, risk assessments, standardization unit operations modules, technical reports, and laboratory procedures.
  • Train Process Development and/or Process Engineering and Manufacturing staff members.
  • Drive timely decisions and facilitate active cross‑functional technical communication and information flow between team members.
  • Support technology transfer related activities for NPI and implementation of process changes into manufacturing from a technical perspective.
  • Partner with Process Engineering and NPI teams to identify and drive process optimization initiatives and address opportunities for efficiency and capacity improvements in all areas of internal and external manufacturing.
  • Author IND, NDA, and other technical documents for regulatory agency submission in support of manufacturing process development activities and serve as process subject matter expert in client and health authority interactions.
  • Use engineering approaches to develop solutions to manufacturing process deficiencies.
  • Perform multiplexed cell‑based assays (killing assays, mixed lymphocyte reactions, proliferation assays, etc.) for process assessment and product characterization.
  • Provide leadership to more junior team…
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary