The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. Based in Visp, you will lead the assigned group of PD/MSAT/DSP Chemists working on pipeline development and portfolio optimization of Drug Linker and Toxin products. You will also play a significant role in the set up of the Drug Linker Development unit Organization for the Drug Linker Asset under construction. This is a highly visible role for a scientist who wants to combine deep technical expertise with people leadership, customer-facing scientific impact, and strategic contribution to a growing Drug Linker Development and Manufacturing organization in the ADC market. This is a fully site-based role, supporting close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
Tasks
- Support the Drug Linker Development Organization Head in the ramp up phase of the Accelerate Asset Development unit by defining and supporting the implementation of all critical business processes for drug linker projects.
- Manage the hiring process of the Accelerate Chemists for the Drug Linker Accelerate Asset together with the DL Development leadership team.
- Lead the assigned Drug Linker Process Development team of Chemists in line with agreed objectives and commitments and monitor and control their performance.
- Support the responsible Drug Linker Development Organization Head, in alignment with the Drug Linker Development Teams, in managing and allocating required chemists and lab resources.
- Guide Development and/or MSAT chemists to enable the efficient and robust transfer of Drug Linker Processes into the supported GMP manufacturing facilities.
- Drive the development and implementation of innovative technologies to increase capability, capacity, and efficiency within Drug Linker Toxin operations and support Lab investment programs for the introduction of relevant technology and tools.
- Act as a technical and scientific expert for Drug Linker Toxin projects internally and externally, including creation of external scientific content to enhance reputation and visibility.
- Facilitate close collaboration between the Drug Linker Development team and critical interfaces and related product areas like Bioconjugates and Small Molecules Operations.
- Lead all HR-related aspects for the assigned team and actively contribute to the scientific development of scientists in their areas of expertise.
- Ensure compliance with GMP and safety regulations throughout all activities.
- Support the Head of Drug Linker Organization in assigned initiatives and strategic duties.
Requirements
- PhD in Chemistry, Chemical Engineering, or a related discipline; PhD in Organic Chemistry preferred.
- Approximately 5-10 years of experience in pharmaceutical process development, API development, clinical supply, or manufacturing sciences.
- Proven experience leading complex projects in a matrix organization within clinical supply, development, or manufacturing operations.
- Strong knowledge of chemical process development, scale-up, technology transfer, and GMP manufacturing requirements.
- Good knowledge of Drug Linker technology and understanding of safe work execution in containment assets.
- People management experience or strong motivation to develop into an expanded leadership role, including coaching and talent development.
- Demonstrated experience managing project budgets and delivering against performance targets.
- Fluent English language skills; German proficiency is a strong asset.
Benefits
- An agile career and dynamic working culture.
- An inclusive and ethical workplace.
- Compensation programs that recognize high performance.
- A variety of benefits dependent on role and location.
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