Elos Medtech is one of the world’s leading development and manufacturing partners for companies in the medical technology sector. With sites in Switzerland, Sweden, Denmark, Germany, China, and the United States, we specialize in the production of implants, instruments, and components for medical technologies. We are looking for individuals who share our values — passion, trust, and results — so we can grow together and achieve even greater success. If you are ready to give your best and join an environment that values collaboration and commitment, we look forward to receiving your application. For our sites in Switzerland, based in Yverdon-les-Bains or Muntelier, we are looking for aWhat we are looking for:Coordinate medical device implementation projects together with R&D, Quality, Operations and our customers, ensuring completion within the agreed scope, timeline, quality

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and budget. Lead and coordinate the project team, fostering effective collaboration and clear communication with all stakeholdersIdentify risks and opportunities during the project and develop appropriate mitigation strategiesDefine and execute validation and

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activities together with Quality Assurance, in compliance with relevant medical regulations (e. ISO 13485, 21 CFR Part 820, MDR) Identify issues and drive continuous improvement actions (productivity, waste reduction, process robustness) What makes you a great fit :Degree in Mechanical Engineering, Medical Technology or another relevant technical fieldExperience in plastic injection processes and/or injection molds, or strong motivation to develop this expertiseExperienced and rigorous in technical data management and ERP system configurationProficient with 3D CAD software (SolidWorks / Creo) English and French are a must, German a strong plusWhy you’ll love working with us:An open and dynamic company culture, short decision-making processes, and an open-door philosophy6 weeks of vacationAttractive social benefitsOpportunities for individual developmentRegular team eventsLoyalty bonuses.

activities together with Quality Assurance, in compliance with relevant medical regulations (e. ISO 13485, 21 CFR Part 820, MDR) Identify issues and drive continuous improvement actions (productivity, waste reduction, process robustness) What makes you a great fit :Degree in Mechanical Engineering, Medical Technology or another relevant technical fieldExperience in plastic injection processes and/or injection molds, or strong motivation to develop this expertiseExperienced and rigorous in technical data management and ERP system configurationProficient with 3D CAD software (SolidWorks / Creo) English and French are a must, German a strong plusWhy you’ll love working with us:An open and dynamic company culture, short decision-making processes, and an open-door philosophy6 weeks of vacationAttractive social benefitsOpportunities for individual developmentRegular team eventsLoyalty bonuses.