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Fujifilm

Global precision manufacturer for healthcare

Production Engineer

Process EngineeringPosted on Nov 5
Full-timeSanta Ana, CA, USA$91.1k - $118.8k

About the Job

Requirements

  • A Bachelor of Science in Chemical Engineering, or a similar scientific/engineering background.
  • Five to seven years of experience in manufacturing engineering, process engineering, project engineering, or a similar role in a current Good Manufacturing Practice (cGMP) environment.
  • Understanding of Good Manufacturing Practice (GMP) regulations and guidelines set forth by regulatory agencies, such as the Food and Drug Administration, for manufacturing life science products.
  • Knowledge and experience working within a quality management system, including investigation resolution, Corrective and Preventative Action (CAPA) implementation, and change control procedures.
  • Familiarity with and ability to apply Lean Manufacturing concepts for waste reduction and process optimization, and Six Sigma quality improvement methodologies.
  • Ability to speak, read, and write in English.

Responsibilities

  • Collaborate with team members to improve processes related to health, safety, and environment.
  • Analyze current manufacturing processes to identify improvement areas and implement solutions that enhance efficiency, quality, and yield.
  • Participate in and troubleshoot production activities on the shop floor, ensuring adherence to established procedures and safety protocols.
  • Collaborate with manufacturing teams to integrate new products and identify and optimize processes for successful production launches.
  • Lead investigations into deviations and non-conformances, and develop and implement corrective and preventative actions to minimize future occurrences.
  • Use process and utility system knowledge to improve equipment functionality and overall manufacturing efficiency.
  • Support implementation of new production equipment, including design, procurement, cGMP documentation, commissioning, and qualification activities.
  • Propose, write, review, and revise departmental Standard Operating Procedures (SOPs) to ensure clarity, consistency, and quality in production practices.
  • Work cross-functionally to maintain and improve the accuracy of Bills of Materials (BOMs) and Electronic Batch Records (EBRs) for existing products, and provide technical feedback and ensure completeness during setup of new parts and processes.
  • Provide technical assessment and ensure manufacturing impacts are captured during the management of change process.

Desired Qualifications

  • Prior experience working with a variety of bioprocessing equipment in a GMP manufacturing environment is highly preferred.
  • Prior experience in the life sciences industry is a plus.

About the Company

Fujifilm

Global precision manufacturer for healthcare

Fujifilm is the main operating and manufacturing arm of the Fujifilm group, turning precision chemistry, nanotechnology, and optical engineering from the film era into products for deep tech and life sciences. It runs Bio CDMO facilities that manufacture complex biopharmaceuticals and vaccines, and its materials division makes photoresists and chemical slurries essential to semiconductor and display production. In healthcare, it develops AI-powered imaging devices, endoscopes, and ultrasound systems, while also serving consumers with INSTAX instant photos and X-Series cameras. Its goal is to translate core technical capabilities into reliable, market-ready products across healthcare, electronics materials, and imaging, maintaining leadership in precision manufacturing and applied science.

Company size
501-1,000
Company stage
IPO
Headquarters
Tokyo, Japan
Founded
1934

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