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The Director, Scientific Office for Genomic Medicine is a scientifically credible, externally facing leader who shapes Cytiva’s innovation agenda in genomic medicine. With a deep understanding of emerging technologies, customer needs, and scientific trends across viral vectors and cell and gene therapy, this role sets and drives Cytiva’s technology vision, strengthens external scientific presence, and serves as a senior expert across genomics, cell therapy, and gene therapy. Acting as a bridge between science, strategy, and execution, the Director partners closely with R&D, Commercial, Marketing, Product Management, Regulatory, Manufacturing, and BD to translate insights into differentiated innovation, next‑generation products, and strategic collaborations that reinforce Cytiva’s leadership in genomic medicine.
Job Responsibility:
Shape Cytiva’s scientific and technology vision for genomic medicine, guiding innovation strategy and next‑generation product roadmaps across viral vector and CGT technologies
Lead early‑stage innovation scouting by identifying emerging science, platforms, and disruptive technologies that inform future product and platform evolution
Serve as Cytiva’s external scientific ambassador, representing the company at key conferences, advisory boards, and scientific networks to strengthen visibility and influence
Build and nurture strategic collaborations with academia, biotech, and ecosystem partners to accelerate scientific leadership and technology development, ensuring business impact
Provide scientific expertise across genomics, viral vectors, cell therapy, and gene therapy to guide R&D, commercial, BD, and strategic teams
Translate customer and market insights into clear internal guidance, identifying unmet needs, technology trends, and business opportunities to shape portfolio and partnership decisions
Drive cross‑functional alignment across R&D, manufacturing, marketing, regulatory, and commercial functions to ensure cohesive and market‑backed technology execution
Deliver scientific communication and thought leadership, influencing executive decision‑making and elevating Cytiva’s profile through publications, presentations, and digital content
Requirements:
PhD (preferred) or Master’s degree in Molecular Biology, Virology, Genetics, Cell Biology, Biomedical Engineering, or a closely related life‑science field
10+ years of experience in biopharma, biotechnology, or the cell & gene therapy/viral vector ecosystem, including exposure to innovation, R&D, or advanced technologies
Deep scientific expertise in viral vectors (AAV, LV, viruses) and cell therapy platforms, with strong understanding of upstream, downstream, and analytical workflows
Demonstrated experience with early‑stage innovation, technology scouting, or evaluating emerging scientific/technical trends relevant to genomic medicine
Familiarity with industry‑standard scientific tools and systems, such as ELNs/LIMS, sequence/design platforms (e.g., SnapGene, Benchling), and data analysis tools (e.g., Prism, JMP)
Cross‑functional R&D or product development exposure, ideally collaborating with Manufacturing, Commercial, Regulatory, and Business Development teams on scientific or technical programs
Proven experience interfacing with external scientific ecosystems, including academic groups, biotech innovators, consortia, or technology/industry forums