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You will lead and inspire a team of approximately 10 scientists (a mix of Research Engineers/PhDs and Technicians) dedicated to the design, optimization, and scale-up of synthetic processes for future drug candidates. Operating at the interface between
In this role you will provide strategic leadership across key quality functions, ensuring our products consistently meet the highest standards of quality, safety, and compliance. You will play a pivotal role in product release, regulatory compliance,
Lead technology transfers and regulatory submissions while managing multiple programs in line with CMC objectives and timelines. Apply Best Product at Pivotal and Speed to the Clinic principles, prioritize resources across competing programs, and ensure
Develop and implement the Global Medical Affairs plan for PsO aligned with biologics portfolio strategy, with emphasis on post-launch lifecycle optimization; Ensure tactical execution of medical plans within agreed global priorities and governance
Ensure execution of the Global Medical Affairs plan and tactics. Review and validate local medical affairs plans from operating countries. Medical lead for strategic planning across the product lifecycle, including launch readiness for new indications and
In this role, you’ll shape the future of our global biosimilar pipeline. You’ll sit at the crossroads of science, commercial strategy, and investment decisions - helping determine which biosimilar assets we invest in, when, and at what scale