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 site in Muntelier and Yverdon-les-Bains, we are looking for aQuality Manager 100%What we are looking for:Quality Manager (Quality Management Representative) for the certified, harmonized Quality Management System (QMS) across two sitesPeople management of the QA team in Muntelier and Yverdon (work at both sites)Overall responsibility for quality-related activities at Yverdon and Muntelier and leadership of the local QA organizationEnsuring the implementation, maintenance, and continuous improvement of the QMS in compliance with ISO 13485, FDA 21 CFR Part 820 and applicable national and international regulationsLeading and coordinating internal, customer, and notified body audits, including preparation, execution, and follow-up activitiesActing as the primary contact for customers, notified bodies, authorities, and business partners on quality-related mattersOverseeing core QA processes including complaints handling, CAPA, change management, and audit managementReporting on QMS performance and key quality indicators to top management and Global QA, and driving continuous improvement initiativesManaging QA resources, including team leadership and budget responsibility, in alignment with global and local policiesSupport in Regulatory Affairs for internal projects and customer requestsWhat makes you a great fit?:Technical background (ES, HES) with continuing education in quality managementExperience in regulatory affairs is preferredProven experience in quality assurance within a MedTech productionExperience in team managementOngoing training in lean managementStrong interest in and understanding of technical topicsConfident and competent communicator, able to interact effectively with internal departments as well as with customers and suppliersGood knowledge of MS Office and experience with CAQ and ERP systemsBilingual French and German, good written and spoken English; Whyyou'll love working with us:An open company culture, short decision-making processes, and an open-door philosophy6 weeks of vacationAttractive social benefitsOpportunities for individual developmentRegular team eventsLoyalty bonuses j4id10187878a j4it0418a j4iy26a