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Site Head, Viral Gene Therapy - Boston

Employer
FUJIFILM Diosynth Biotechnologies
Location
College Station, TX
Start date
Aug 1, 2022
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Job Details

Summary:

A unique opportunity to lead a new state-of-the-art process development and manufacturing facility for viral vectors and advanced therapies in the greater-Boston area.

As a leading global Contract Development and Manufacturing Organization, FDB continues to grow and further accelerate offerings in viral vectors and advanced therapies. We are looking for a people, business, and technically savvy Head of Site, ready to embark on a new journey with us as well as to recruit and lead a high performing organization. The new facility will house experimental and analytical equipment for viral vector and advanced therapy process development, with contract manufacturing services for early phase clinical trials beginning at the site in fall 2023.

The Site Head will provide strong scientific, business and administrative leadership to Viral Gene Therapy process development and early stage cGMP manufacturing group at the Boston site, setting annual goals and objectives and long range planning.  The Site Head will provide high-level business strategy for the site, oversee the management of resources and coordinate activities across multiple departments to achieve business objectives and revenue goals.  This individual will serve as the strategic leader and an advocate for the site to the Viral Gene Therapy leadership team and will work to enhance the existing and establish new collaborations within the academia, pharma and industry communities to perform cutting-edge research and innovation in the field of advanced therapies.

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Essential Functions:

The job holder will build, inspire, lead, and manage Viral Gene Therapy process development and early stage cGMP manufacturing group at our Boston site.

  • Lead the establishment of the facility and the team, including hiring of staff and capital deployment enabling a fully functional service offering from the Boston site
  • Ensure competitive excellence in VGT process development and manufacturing science.
  • Ensure the effective operation, organization, and delivery of site VGT business targets.
  • Ensure the team works safely within FDB's EH&S policies
  • Ensure the team operates within the FDB Quality Management System.
  • Engage and align with the global FDB Viral Gene Therapy science and manufacturing communities, aligning and standardizing operations, procedures and customer experience where feasible.
  • Contribute, support and collaborate with the Viral Gene Therapy Business Steering Group on behalf of the site
  • Support the sales and marketing activities to attract secure, and retain client programs
  • Develop and grow the technical contacts and relationship with the local community on behalf of FDB.

Minimum Qualifications:

  • Ph.D. degree preferably in Chemistry, Biology, Life Sciences, or related field, with at least 12 years' GMP experience preferably in the pharmaceutical or biotechnology industry of which at least 5 years of management/supervisory experience OR;
  • Master's degree in Chemistry, Biology, Life Sciences, or related field with at least 16 years' GMP experience preferably in the pharmaceutical or biotechnology industry of which at least 5 years of management/supervisory experience. 

Preferred Qualifications:

  • Matrix management experience.
  • Previous experience in a Contract Manufacturing Organization (CMO) environment

We are an equal opportunity and affirmative action employer.  All qualified applicants will receive consideration without regard to race, color, national origin, sex, gender identity, sexual orientation, religion, disability, protected veteran status or any other characteristic protected by applicable federal, state or local law. 

If an accommodation to the application process is needed, please e-mail FDBTHR@fujifilm.com or call 979-431-3500.

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Company

FUJIFILM Diosynth Biotechnologies is an industry leading cGMP Contract Development and Manufacturing Organization (CDMO) supporting our partners in the biopharmaceutical industry with the development and production of their biologic, vaccines and gene therapies.

With over 30 years of experience in process development and cGMP manufacturing, a dedicated staff of over 2,000 and a reputation for excellent customer service, flexibility and responsiveness, we’ve become a trusted partner to some of the most prominent biotech developers and pharmaceutical companies in the industry.

Our Process Development experience includes the development of processes for molecules expressed via fermentation (e.g., E. coli, P. pastoris), cell culture systems including CHO, HEK, Vero, MDCK, EB66 and insect cells, and from transgenic sources.

Our network expands within five development and manufacturing facilities located in Teesside, United Kingdom; Research Triangle Park, North Carolina, USA; College Station, Texas, Thousand Oaks CA USA and Hillerød, Denmark.

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Find Us
Website
Phone
919-337-4400
Location
Thousand Oaks, CA
Research Triangle Park, NC
College Station, TX
Holly Springs, NC
Watertown, MA
United States
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