About The Position

Join a high-impact team shaping end-to-end biologics programs for clients across the globe. As an Associate Director or Director in Program Design, you’ll lead technical engagements, design robust development-to-cGMP manufacturing strategies, and craft compelling, client-tailored proposals that accelerate new business for FUJIFILM Biotechnologies. You’ll partner closely with our global commercial organization and site technical/operations teams to translate complex science into executable, high-value programs. This role is ideal for a seasoned technical leader from a CDMO or biopharma environment who thrives at the intersection of science, strategy, and client engagement.

Requirements

  • A B.S. degree, preferably a graduate degree (e.g. MSc, PhD), in a relevant biological science field.
  • 8+ years of related technical experience at Fujifilm, other CDMO, or other applicable role, including experience working directly with customers.
  • 4+ years’ experience managing, leading and developing leaders (Managers/Supervisors).
  • 6+ years of experience in pharmaceutical/biological manufacturing operations.
  • Broad understanding of FUJIFILM Biotechnologies or relevant CDMO business, with special focus on Biologics (Microbial and/or Mammalian) manufacturing.
  • Understanding of regulatory environment, process development, and analytical technologies related to the manufacture of biopharmaceutical drugs.
  • Understanding of and experience with cGMP manufacturing and associated requirements.
  • Excellent written and verbal communication skills with the ability to interact with external customers in a professional and personable manner and to present a competent image of FUJIFILM at all times.
  • Ability to analyze complex technical problems and present clear solutions.
  • Ability to influence customers and colleagues at all levels.
  • Any combination of education and experience, which would provide an equivalent background to deliver against role expectations.

Nice To Haves

  • Prior experience within FUJIFILM a plus but not required.
  • Credibility in bioprocess development, tech transfer, and cGMP manufacturing environments.
  • A consultative, solutions-oriented approach with the ability to translate technical complexity into clear, actionable program designs.
  • Comfort operating in a fast-paced, highly cross-functional and customer-facing role.
  • For Director: demonstrated leadership of initiatives and people, with a track record of harmonizing processes across sites or teams.

Responsibilities

  • Lead the technical aspects of customer meetings and teleconferences, projecting FUJIFILM’s experience and expertise.
  • Review RFPs and design end-to-end customer programs spanning tech transfer, cGMP manufacturing, and process validation.
  • Assess customer programs for technical fit with FUJIFILM capabilities and site requirements; advise optimal siting, scope, and timelines.
  • Partner with process sciences, engineering, and Quality teams to evaluate technical pathways and operational feasibility.
  • Develop and author high-quality, customer-tailored proposals and statements of work.
  • Support the full sales cycle, including Stage Gates, Win Rooms, and ongoing customer requests.
  • Maintain strong internal stakeholder engagement to promote open communications and continuous improvement of service offerings.
  • Stay current with industry advancements; represent FUJIFILM at webinars and conferences.
  • Director level: lead Program Design improvement initiatives and harmonization of work practices across sites; may manage 1–3 direct reports.

Benefits

  • Competitive compensation and benefits
  • professional development
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