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Are you a high-caliber grant strategist who thrives at the intersection of complex bioprocessing and non-dilutive capital? If you are ready to transition into a fast-paced, high-growth environment modeled after the world’s leading cell and gene therapy accelerators, this is your next move. We are looking for a technical powerhouse who understands that moving a therapy from bench to bedside requires more than just a lab, it requires the strategic orchestration of Horizon Europe, Vinnova, and EIC funding to fuel a world-class CDMO infrastructure.
Job Responsibility:
Portfolio Strategy: Identify, prioritize, and capture high-value funding streams from Vinnova, Horizon Europe, and Eurostars
Technical Synthesis: Translate complex CDMO operations into high-precision technical proposals
Consortium Leadership: Build and lead cross-functional consortia involving Tier-1 academic institutions, clinical trial units, and industrial partners
Project Lifecycle Management: Oversee the administrative and technical reporting requirements for secured grants
Stakeholder Liaison: Act as the primary technical point of contact for funding agencies and regulatory bodies
Requirements:
Ph.D. in Biotechnology, Molecular Biology, Immunology, or a related Life Science field
Deep understanding of the ATMP regulatory landscape (EMA/FDA) and GMP manufacturing requirements
Minimum 6+ years of experience in high-stakes grant writing or strategic consulting within the Life Science sector
Expert-level knowledge of Horizon Europe’s Work Programmes
Exceptional technical writing skills in English
Nice to have:
A dual degree in Business (MBA) or Law (LLM) is a significant advantage