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Fujifilm

Global precision manufacturer for healthcare

Quality Assurance Specialist 3

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeBryan, TX, USA$65k - $88.2k /yrIn-person

About the Job

Requirements

  • A Master's degree in Biology, Chemistry, Engineering, or a related field and one year of experience as a quality assurance specialist or in a related quality assurance occupation; alternatively, a Bachelor's degree in one of those fields and three years of relevant experience.
  • Quality assurance experience in the pharmaceutical or another regulated industry.
  • Experience presenting during audits and inspections.
  • Experience building and leading training content related to quality system records.
  • Experience using a digital Quality Management System platform.
  • Technical writing experience.
  • Previous experience in a position where current Good Manufacturing Practice (cGMP) regulations govern production of drug, biologic, or vaccine products.

Responsibilities

  • Review and approve Quality System Records, including deviations, corrective and preventive actions (CAPAs), and complaints, in compliance with company quality policies and site standard operating procedures to ensure regulatory compliance.
  • Track, coordinate, remediate, and close deviations, CAPAs, and complaints.
  • Maintain daily metrics for pending deviations, CAPAs, and customer and client complaints to support on-time closure.
  • Provide quality oversight of deviations, CAPAs, and customer complaints, and write up client complaints to ensure root-cause analyses and investigation write-ups are clear and concise.
  • Conduct timely information-gathering sessions with cross-functional departments to obtain information and data needed to review and close investigations.
  • Support client due diligence, quality audits, regulatory inspections, and client audit requests.
  • Work with Quality management to implement and grow phase-appropriate quality systems that enable cGMP manufacturing of pre-clinical through commercial products.
  • Ensure personal and team training and site actions are not overdue.
  • Support other Quality Assurance teams and other functions in completing site actions.
  • Provide cGMP assistance to cross-functional departments, including Facilities, Materials Management, Quality Assurance, and Validation.
  • Promptly notify Senior Management of potential quality or regulatory issues that may affect product quality or regulatory compliance.

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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