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• Design and implementation of experiments investigating statistical learning and predictive processing using intracranial EEG and intracortical microstimulation in human epilepsy patients
• Analysis of intracranial electrophysiological recordings using modern computational and statistical approaches

• Form and optimize SLBs on Si/SiO₂ chips (surface prep, lipid/buffer conditions, QC).
• Functionalize SLBs for protein attachment (e.g., His-tag/Ni-NTA, biotin–streptavidin, other orthogonal chemistries).

• Own EU CMC regulatory strategy for assigned clinical-stage programs (phase I–III).
• Serve as regulatory partner to Quality and Technical Development, ensuring alignment while maintaining a risk-based regulatory perspective.

Global Scientific Manager - IBU Critical Care Become part of a vital chain and contribute to our common goal of making people’s lives better. Headquartered in Lachen, Switzerland, Octapharma is one of the largest human protein manufacturers in the world, developing and producing medicines sourced...

• Conduct and development of statistical analysis of cohort study, proteomic and multiomics data and their links to disease phenotypes
• Interpretation and interdisciplinary discussion of research results

Lead of Medical Scientific Information, International 100%...

• Hands-on experience building foundations for realtime simulation systems
• The chance to learn, implement and extend state-of-the-art simulation methods (XPBD, advanced constraint solvers, hybrid models)
• Mentorship from PhD-level researchers

Director MedTech Consulting & Business Development – Switzerland (m/w/d) seleon GmbH, a part of ai6 Solutions, is a leading service partner for medical technology companies in Central Europe for around 30 years, with a focus on development, regulatory consulting, and production. We support MedTech...

Medical Science Liaison Oncology - Schweiz Mitte (Ref. 2754) - (BS/BE/SO/AG/Zentralschweiz) Our client is a well‑established, globally active pharmaceutical company with a strong footprint in the Swiss market and a diverse portfolio of innovative therapies across several specialty areas. As part of...

• Lead the planning, execution, and coordination of sterile product development in the formulation lab, focusing on parenteral small molecule and peptide dosage forms.
• Design, review, and recommend changes to scientific protocols and procedures for aseptic processing and sterile manufacturing.

Providing strategic regulatory guidance developing global regulatory strategy, planning and execution of global investigational and marketed prescription drug submissions and managing lifecycle regulatory activities in alignment with the Therapeutic Area Lead under the direction of the Senior...