Director, Cell R&D

Director, Cell Based R&D

Responsible for defining and executing the scientific and technical strategy for Aldevron’s and IDT’s cell-based platforms such as plasmid DNA and recombinant protein manufacturing. Reports to the VP, Platform Development, Biology and Analytical and is part of the R&D Leadership Team. On-site role in Fargo, ND or Waltham, MA.

• Lead innovation and development across Aldevron’s cell-based platforms, including plasmid, nanoplasmid, nanoplasmid backbone, and recombinant protein technologies.
• Set research priorities, allocate resources, and define scientific outcomes that support strategic business goals and pipeline advancement.
• Oversee key discovery experiments and development processes to achieve critical product and process milestones.
• Build, mentor, and lead a high-performing interdisciplinary R&D team, fostering collaboration, development, and accountability.
• Drive strategic plans for new products, process improvements, testing, and emerging technologies in molecular biology and protein R&D.
• Serve as the technical leader for core product and process initiatives, contributing to intellectual property development and maintaining industry leadership.
• Partner cross-functionally and engage directly with clients and external stakeholders to align requirements, support business growth, and identify new opportunities.

• Doctoral degree (Ph.D.) in a scientific discipline related to Aldevron’s core business (Biology, Biochemistry, Genetics, Chemistry, etc.) and/or a Doctor of Medicine degree (M.D.).
• 12+ years of leading corporate R&D and new product development (NPD) or otherwise providing scientific leadership in an industrial setting.
• Track record of leading research collaborations with academia and industry.
• Experience leading teams, including direct supervision of researchers.
• Proficiency in cloning techniques, DNA, RNA and protein experience.
• Proven track record of creative scientific accomplishment as evidenced by publication and/or patent record.

• Track record of supporting programs from research to clinic.
• Experience supporting GMP environments.

Ability to travel up to 25%.

Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The U.S. EEO posters are available here. We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact: or