Technical Leader

The Technical Leader for Quality Control will be responsible for overseeing and guiding the technical work performed by a team of analysts in the biopharmaceutical sector. This role will focus on analytical release and stability testing of monoclonal antibodies (mAbs) gene therapy products for both drug substances and drug products. The ideal candidate will possess a deep technical background strong leadership skills and a passion for fostering innovation and excellence within the QC team.

The work we do at FUJIFILM Diosynth Biotechnologies has never been more importantand we are looking for talented candidates to join us. We are growing our locations our capabilities and our teams and looking for passionate missiondriven people like you who want to make a real difference in peoples lives. Join FDB and help create the next vaccine cure or gene therapy in partnership with some of the most innovative biopharma companies across the globe. We are proud to cultivate a culture that will fuel your passion energy and drive what FUJIFILM Diosynth Biotechnologies call Genki.

College Station Texas may be a small university town but the lively cultural scene and local amenities make it a great place for families as well as those who want the ease of smalltown life and the convenience of living close to the vibrant pulse of big cities. Eightyseven percent of Texas population lives within a 180mile radius so we are in the center of it all in Texas. And our site is nestled in the hub of innovation representing a source of pride for the area.

Key Responsibilities:

• Provide expert guidance on analytical methodologies and techniques relevant to mAbs gene therapy including but not limited to:
  • Chromatography (e.g. HPLC SEC IEX RPHPLC)
  • Mass Spectrometry (e.g. LCMS MALDITOF)
  • Electrophoresis (e.g. SDSPAGE capillary electrophoresis)
  • EnzymeLinked Immunosorbent Assay (ELISA)
  • Nucleotide and protein quantification (e.g. qPCR UVVis spectrophotometry)
  • Cellbased assays (e.g. cytotoxicity assays cell proliferation assays and receptor binding assays)
  • Flow cytometry for analyzing cell populations and assessing phenotypic and functional characteristics.
  • Visual inspection techniques for particulate matter and container closure integrity.

• Facilitate training and development for team members enhancing their technical skills and knowledge in QC practices.
• Collaborate with scientists and crossfunctional teams to troubleshoot and optimize analytical techniques.
• Actively monitor method performance metrics identifying trends and areas for improvement.
• Lead troubleshooting efforts for any analytical issues employing root cause analysis to determine underlying problems and implementing effective corrective actions.
• Establish and maintain method performance verification protocols to ensure ongoing compliance with regulatory standards.
• Conduct comprehensive reviews of analytical data to assess consistency accuracy and reliability across different testing modalities.
• Integrate findings from various assays and methodologies to provide a cohesive evaluation of product quality and performance.
• Ensure that data reviews align with regulatory requirements and industry best practices supporting informed decisionmaking.
• Champion data integrity initiatives ensuring that all analytical data is generated recorded and maintained in accordance with ALCOA principles (Attributable Legible Contemporaneous Original Accurate and Complete).
• Implement and monitor systems and practices that ensure the reliability and quality of data throughout its lifecycle.
• Identify and implement process improvements within the analytical framework to enhance efficiency and reliability of testing.
• Foster a culture of continuous improvement encouraging innovation and adoption of best practices within the QC team.
• Conduct regular audits of data management practices identifying areas for improvement and ensuring compliance with regulatory standards.
• Work closely with crossfunctional teams including R&D manufacturing and regulatory affairs to ensure alignment on analytical requirements and timelines.
• Communicate technical findings and updates to senior management and stakeholders translating complex data into actionable insights.
• Review and approve analytical data ensuring accuracy and compliance with regulatory expectations.
• Manage investigations of deviations and outofspecification results implementing corrective and preventive actions as needed.
• Stay updated on regulatory changes and industry trends ensuring the QC team is prepared for inspections and audits.
• Participate in regulatory submissions and provide technical input as required.
• Ensure comprehensive documentation of all analytical procedures and results maintaining compliance with GMP and GLP standards.
• Prepare and present technical reports and presentations for internal and external stakeholders.

Qualifications:

• Masters or PhD in a relevant scientific field (e.g. Biochemistry Biology Chemistry).
• 8 years of experience in quality control within the biopharmaceutical industry with a strong focus on analytical testing.
• Proven expertise in analytical methodologies related to mAbs gene therapy products with handson experience in relevant analytical techniques.
• Exceptional leadership and interpersonal skills with a track record of mentoring technical teams.
• Strong problemsolving abilities and a keen attention to detail.

Fujifilm is committedto providing equal opportunities in hiring promotion and advancement compensation benefits and training regardless of nationality age gender sexual orientation or gender identity race ethnicity religion political creed ideology national or social origin disability veteran status etc.

If you require reasonable accommodation in completing this application interviewing completing any preemployment testing or otherwise participating in the employee selection process please direct your inquiries to our HR Department or.