True to the vision "We drive innovation to improve people's lives", the Hamilton companies have been providing solutions for the health sector since 1950. We are an innovative pioneer in the fields of ventilators, automated pipetting, sample management and in the development of process sensors. We are an innovative pioneer in the fields of ventilators, automated pipetting, sample management and in the development of process sensors. medin is a subsidiary of Hamilton Medical which develops and produces nCPAP systems and consumables for respiratory support of premature and newborn babies. Hamilton Medical is a leading manufacturer of intelligent ventilators. Whether in intensive care units, during rescue transports or during an MRI examination - our solutions cover a wide range of patient groups, applications, and environments. How you can make a difference : As part of Hamilton Medical, we develop and distribute innovative nCPAP systems worldwide for clinical use in the delivery room, during transport and in the intensive care unit for premature and newborn babies. To support our growth, we are seeking a detail-oriented and driven Medical Device Engineer with a focus on product testing to join our dynamic team. In this role, you will be responsible for overseeing and further developing the testing and validation processes of our medical devices, ensuring compliance with regulatory requirements, and contributing to continuous improvement initiatives throughout the product life cycle. Key Responsibilities: Testing and Validation: Develop and execute comprehensive testing protocols for new and existing medical devices, including usability, performance, and safety assessments Regulatory Compliance: Ensure all testing activities meet regulatory standards (FDA, ISO, MDR, etc.) and maintain accurate documentation for compliance purposes Life Cycle Management: Collaborate with cross-functional teams to evaluate the product life cycle, identifying opportunities for enhancements and risk mitigation Data Analysis: Analyze testing data and generate reports that provide actionable insights to stakeholders, facilitating informed decision-making Collaboration: Work closely with Product Management, QRA, and manufacturing teams to ensure seamless integration of testing results into the product development process Continuous Improvement: Participate in initiatives to enhance testing methodologies and processes, driving quality improvements and efficiency gains That’s what you bring along : Bachelor’s degree in Engineering, Biomedical Engineering, or a related field (Master’s degree preferred) 3 years of experience ideally in engineering, life cycle engineering or product testing within the medical device industry Strong understanding of regulatory standards and requirements relevant to medical devices (e.g., FDA, MDR, ISO 13485) Proven experience in developing and executing testing protocols. Strategic and entrepreneurial planning and thinking Goal- and problem-solving-oriented action as well as an independent, pragmatic but methodical and structured way of working A cross-functional understanding and enjoyment of working in an interdisciplinary team Very good written and spoken German and English skills Learn more about career opportunities at Hamilton at jobs.hamilton.ch. Do you share our values and feel at home in a cooperative and down-to-earth environment? At Hamilton, we not only offer a motivating working environment, but also various leisure activities and modern working conditions. Our interactions at eye level encourage open communication and a pleasant working environment. Become part of a team where your skills are valued and innovative ideas are fostered. Interested? Then apply online using the "Apply now" button. If you have any questions, please contact us at jobshamilton.ch with the following details: Reference: JR-4294/Contact: Sarah Halbig Applications by post or e-mail can unfortunately not be considered.