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Quality System Engineer- Medical Devices Quality System Engineer- Medical Devices: Software Engineering / Medical Device / Pharmaceutical Industry / GCP / GXP / ISO 14155 / ISTQB / ISO / IEC 27001/ CFR Part 820/CSV, MDR, CE , 510(k)/ Clinical Investigations / Englisch Projekt: For our client, a...

Senior Specialist Metabolic Health - Hormone Regulation The Nestlé Group is the world's largest food and beverage company with 92.6 billion Swiss Francs in sales in 2019. It is present in 187 countries around the world, has 403 factories and its 291'000 employees are committed to Nestlé's purpose...

• be part of powerful agile team of software engineers
• dive deep into the existing infrastructure applications and their architecture
• maintain and modernize them to make sure they stay state-of-the-art
• ensure high-quality software by adequate software design, data structures and good code test coverage

RESEARCH ASSOCIATE (m/f/d) The Family Larsson-Rosenquist Foundation is a non-profit organization dedicated to supporting and promoting breastfeeding and breastmilk. Our work is international, science-based, and carried out in collaboration with global experts. Together, we build publicly available,...

Develop and define formulation strategies for protein drug candidates across all development stages, including stability assessment, excipient selection, and container-closure compatibility...

Assess the environmental fate and risk of products of Sasol International Chemicals in connection with their development, production, marketing, utilization and disposal and identify and develop strategies to mitigate potential risks...

Senior Biomedical R&D Engineer (90-100%) machineMD is a Bern-based medical device company pioneering automated neurodiagnostics through our flagship neos™ device and oculometrics software. We're growing our R&D team and adding a Senior Biomedical R&D Engineer – Oculometrics & Neurodiagnostic...

• Independent work on a doctoral project on the research topic “radiobiological experiments with proton beams in the magnetic field of an MR Scanner”
• Conducting systematic literature research and summarizing the current state of knowledge

• Planning and execution of pre-/post-market clinical studies (vascular, oncology); ensure deliverables are completed on time and within budget.
• Provide regular reporting of metrics to Clinical Affairs leadership.

• Develop embedded software for medical devices, ranging from low-level drivers to higher-level functionalities and embedded UI
• Take technical ownership of features and contribute to architecture, design, implementation, and testing

• Design and conduct longitudinal analyses linking autonomic measures (cardiac vagal control, sympathetic activity) to health, brain, and molecular biomarkers.
• Build and maintain reproducible pipelines to clean, harmonize, and integrate multi-modal data across waves and cohorts.