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• Act as the Responsible Person (RP) / Fachtechnisch verantwortliche Person (FvP) in accordance with Swiss regulatory requirements (HMG, AMBV) and Swissmedic Technical Interpretation .17.
• Ensure compliance with applicable GMP requirements and regulatory commitments across manufacturing operations.

• Develop melt-spun liquid/gel-core fibers with polyolefin sheaths and functionalized, hydrophobic cores
• Explore selective scavenger systems for transition metal (TM) ions and HF, including chelating ligands, reactive nanoparticles and additives

You represent the full scope of Digital Production Technologies teaching and research, with a particular focus on modern manufacturing and production systems, their planning, control, and automation, as well as simulation- and data-driven methods in digital production....

Development, optimization and upscaling of GMP-compatible manufacturing processes for lyophilization of biologics (e.g. Anti-body drug conjugates, ADCs), incl. preparation and documentation of development activities...

Team Leadership & Development: Lead, mentor, and develop a high-performing team of MSAT specialists. Drive the efficiency, structure, and continuous improvement of the group's operations....

• Contribute biological expertise and domain knowledge to the development, validation, and implementation of AI-supported candidate gene discovery approaches.
• Identify, analyse, integrate, and interpret complex multi-omics datasets to support candidate gene discovery and trait development.