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• Perform integrative analyses combining multi-omics data with eye imaging data
• Contribute to ophthalmic data collection and processing
• Contribute to omics data processing, statistical analyses, and the preparation of manuscripts for publication in peer-reviewed journals

• Help build the foundation for next-generation products
• Learn and apply cutting-edge simulation methods
• Receive mentorship from experienced PhD-level experts
• Explore the opportunity to write your master's thesis after your internship or working student role

You will begin your work with an in-depth analysis of the current state of research and lay the strategic foundation for the project by comprehensively researching and evaluating diverse assay technologies, from innovative recognition molecules to advanced coupling and detection strategies....

With your PhD thesis you bring life into technology by developing automated isolation, enrichment and library preparation techniques from diverse clinical specimens which are relevant for Next-Generation Sequencing (NGS) analyses in the field of precision medicine....

Senior Analytical Manager Pharmacopeia Solutions As Senior Analytical Manager for our Pharmacopeia Solutions team, you lead a laboratory group responsible for compendial and routine analytical testing, including titration, raw material testing, and water content analysis ( ). You ensure efficient,...

• CRISPR based drug screening of freshly derived human glioblastoma
• Development of computational analytical tools
• Analysis and tackling of resistance mechanisms
• Development of a drug decision algorithm based on clinical and preclinical evidence

Field Application Scientist - China Focus The cutting-edge electrophysiology platforms of MaxWell Biosystems enable scientists in pharmaceutical industries, contract research organizations, and academia around the world to characterize the function of neurons and the effect of compounds. Our...

• Support GxP compliance of all activities in the clinical trial supply management, drug-related distribution and storage
• Responsibility for the project-related GxP documentation and maintenance of lists

Support of planning, managing and steering of timelines, costs and scope of Trial Teams for agreed deliverables of global supply chain activities for assigned clinical trials, including highly complex trials...

• Independently lead cross-functional teams through the full product lifecycle-from concept to market launch, ensuring alignment with business strategy.
• Lead and deliver complex hardware and software automation development programs with global impact.

We are looking for Clinical Affairs Managers within the cutting edge Medical Device industry, based in Bern Medical Device/Clinical Affairs Manager Tasks Planning, execution, and management of clinical studies from A to Z Preparation and review of all types of clinical study documents Preparation...

• Mass spectrometry-based lipidomics
• LC-MS/MS analyses and lipid annotation
• Mass spectrometric imaging (MS Imaging)
• Data analysis and integration

Lead the Engineering Testing & Laboratory team (ETAG) at AbbVie Ludwigshafen Device & Combination Product Development....

Research Associate (Biology, 100%, m/f/d) NBE-Therapeutics is a subsidiary of the Boehringer Ingelheim group (BI): a perfect symbiosis between a rapidly growing biotechnology company and an already well-established big pharma. We are located in Basel, a Swiss city on the river Rhine, known for...

• Lead and collaborate with cross-functional teams to develop AI-driven biomarker signatures for target engagement, patient stratification, and early biological activity
• Design and apply computational pathology and AI approaches across diverse tissue types, disease areas, and clinical endpoints

Lead and collaborate with cross-functional teams to generate digital biomarker signatures from complex datasets using AI/machine learning, enabling target engagement assessment, patient stratification, and early signals of biological activity....

• Driving scientific marketing initiatives by aligning clinical insights with business objectives and supporting market entry and adoption across EMEA
• Leading and executing clinical studies, including planning, protocol development, monitoring and data analysis for flow cytometry, IHC and PCR

• Build and lead the Viral Vector Operations unit
• Drive process development and GMP manufacturing for viral vector platforms (e.g. Lentivurus, MVA)
• Ensure reliable, scalable, and high-quality GMP execution
• Oversee tech transfer, scale-up, and manufacturing readiness