The Opportunity As Associate Director, Human Factors Design and Development, you will lead the integration of human factors engineering and usability strategies for medical devices, combination products, and healthcare technologies. Your work will ensure that products are
About Us Ikerian AG (formerly RetinAI Medical) is a fast-growing medical device software company headquartered in Bern, Switzerland. Our mission is to enable the right decisions sooner in healthcare, through transformative AI & data management solutions
We are currently looking for a Principal Scientist Tech Ops (CMC Science) to join our global team in Bern. In this position you will be responsible for supporting and executing Chemistry, Manufacturing, and Controls (CMC) strategies
The Associate Director of Technology Transfer & External Partnerships leads the planning and execution of technology transfer activities to external partners, including CDMOs, CMOs, and strategic collaborators. This role ensures successful transfer of processes, analytical methods,
For our global Technical Operations Organization, we are currently looking for a Senior Laboratory Specialist – Analytical Testing (m/f/x) Fullltime / Permanent / CF Level 04 Locations available: Bern The Opportunity Researches and develops innovative medicines
The Senior Laboratory Specialist, Tech Ops researches and develops new medicines for unmet medical needs through innovative medical science from inception, through clinical trials to commercialization. Assesses, monitors and ensures products meet clinical safety standards. Conducts sophisticated analysis,
Researches and develops new medicines for unmet medical needs through innovative medical science from inception, through clinical trials to commercialization. Assesses, monitors and ensures products meet clinical safety standards. Conducts sophisticated analysis, manages research information systems and technical
Responsibilities Development and implementation of the clinical strategy for the entire product portfolio Creation, review and maintenance of Clinical Evaluation Reports (CER) in accordance with MEDDEV 2.7/1 Rev. 4 and MDR Annex XIV Conduct of systematic literature searches and
The Role: In this role you will be responsible for bringing new Drug Delivery Systems through the development process. You will have considerable cross-functional interaction, that includes Quality Assurance, Regulatory Affairs, Packaging, CMC, Clinical and Commercial functions. This
Responsibilities Perform hands‑on system‑level verification and validation testing for complex medical devices integrating software, electronics, mechanics, optics, navigation, and robotics. Execute system integration tests and validation activities, ensuring correct interaction of hardware and software components. Prepare,
Thousands of researchers receive funding from the SNSF to study nature, technology and society. Their findings provide an important foundation for progress and well-being. Our task is to select the best ideas at national level based
The Institute for Medical Education (IML) is a center of excellence in medical education. As a university institution, we work in the fields of research, teaching, service and development and supervise projects at the cantonal, national and
The Laboratory Specialist, Technical Operations designs and implements business experimental processes to enable product research and development. Designs related integrated process and candidate / product team activities and directs technical and operational activities to ensure planned project
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
Your mission Perform hands-on system-level verification and validation testing for complex medical devices integrating software, electronics, mechanics, optics, navigation, and robotics Execute system integration tests and validation activities, ensuring correct interaction of hardware and software components
CSL is seeking a Senior Quality Associate in Bern, Switzerland, responsible for managing deviations, investigations, and change controls within the Clinical Development portfolio. This role ensures compliance with GMP regulations while providing support across Technical Product Development. The ideal
What you can expect Further develop and optimize Spin lock functional MRI sequences at 3T and 7T Conduct phantom testing and human data acquisition Improve post processing and quantitative analysis tools Collaborate closely with clinical and technical
The Amazon Web Services Healthcare and Life Sciences (HCLS) Professional Services (ProServe) team is seeking an experienced Clinical ProServe Cloud Architect (PCA) to join our team in Europe. In this role, youll work directly with pharmaceutical and
The Chief Medical Officer (CMO) for Venous Pressure Solutions will serve as the clinical, scientific, and strategic leader driving the validation, adoption, and scaling of the solution. This executive will oversee clinical positioning, medical affairs, evidence generation, KOL
Position Purpose The Senior Quality Associate is responsible for managing deviations, investigations, CAPAs, product technical complaints and change controls associated with development activities and manufacture of Investigational Medicinal Product within CSL Clinical Development portfolio. To do this, the GMP