Junior QM Manager / QA Specialist – Focus GDP & MDR

Junior QM Manager / QA Specialist (w/m/d) – Focus GDP & MDR Shaping the future of the dental industry together. Abc Dental AG and Condor Dental Research Co. Ltd. are among the established partners of the dental industry. As subsidiaries of the world's leading healthcare company Henry Schein, we combine regional customer proximity with international strength. Together, we support dental practices and healthcare professionals with high-quality products, innovative solutions, and excellent service. Our approximately 100 dedicated employees benefit from a modern working environment, short decision-making paths, and the development opportunities of a globally successful company. To strengthen our QM team, we have the following position to fill in the Zurich or Vouvry area: Junior QM Manager / QA Specialist (w/m/d) – Focus GDP & MDR With perspective to become the Deputy Technically Responsible Person (FvP) Workload: 60% – 100% (by agreement) Focus: Operational QA, GDP Compliance & Medical Technology (MDR) in domestic wholesale Development: Targeted onboarding and qualification to become the officially reported FvP deputy Your area of responsibility QMS Support: You supervise and optimize our existing quality management system for medicinal products and medical devices (according to GDP, MDR, ISO 13485). Compliance & Daily Operations: You monitor compliance with GDP guidelines in domestic wholesale and ensure QMS-compliant document control and archiving. Quality Processes: You independently process deviations, changes (Change Control), complaints, and CAPA measures. Audit Preparation: You support the team in the preparation of inspections by Swissmedic as well as in internal self-inspections. FvP Development Path: You will be gradually introduced to the tasks of the Technically Responsible Person according to AMBV in order to legally take over the role of deputy in the medium term. What you bring with you Education: Completed studies in pharmacy, chemistry, biology or a comparable scientific/technical qualification. Professional Experience: Initial or several years of practice in quality assurance (QA) or in quality management (QM), ideally in the pharmaceutical or medical technology industry. Expertise: Basic knowledge or first points of contact with medicinal product law (HMG, AMBV, GDP) as well as international standards (ISO 13485 / MDR) are an advantage. Language Skills: Business fluent German as well as good French and English skills (important for cross-location cooperation). Way of working: An exact, structured way of working and the motivation to work yourself deeply into regulatory topics. What we offer you Development: A clearly defined development plan with the goal of taking over the official FvP deputy role. Flexibility: Modern employment conditions, flexible working hours and up to 2 days of home office per week. Company Culture: An open company culture with flat hierarchies and a collegial working atmosphere. Team Events: Regular joint activities and team events that will inspire you. Do you feel addressed? Then we look forward to your application! Send your complete application documents including your salary expectations to Claus. For questions about the position, please contact Dr. Kraus directly. Shaping the Future of the Dental Industry Together. Abc Dental AG and Condor Dental Research Co. Ltd. are among the established partners in the Swiss dental industry. As subsidiaries of Henry Schein, the world’s leading healthcare company, we combine regional customer focus with international strength. Together, we support dental practices and healthcare professionals with high-quality products, innovative solutions, and excellent service. Our approximately 100 dedicated employees benefit from a modern work environment, short decision-making processes, and the development opportunities offered by a globally successful company. To strengthen our QM team in the Zurich or Vouvry area, we are looking to fill the following position: Junior QM Manager / QA Specialist (f/m/d) – Focus on GDP & MDR With prospects to become the Deputy Responsible Person (RP / FvP) Workload: 60% – 100% (by agreement) Focus: Operational QA, GDP Compliance & Medical Devices (MDR) in domestic wholesale Development: Targeted onboarding and qualification to officially assume the legal role of Deputy RP Your Responsibilities QMS Support: You maintain and optimize our existing Quality Management System for pharmaceuticals and medical devices (according to GDP, MDR, and ISO 13485). Compliance & Daily Operations: You monitor compliance with GDP guidelines in domestic wholesale and ensure QMS-compliant document control and archiving. Quality Processes: You independently handle deviations, changes (Change Control), complaints, and CAPA measures. Audit Preparation: You support the team in preparing for inspections by Swissmedic or Notified Bodies, as well as conducting internal self-inspections. RP Development Path: You will be gradually introduced to the duties of the Responsible Person (FvP) under Swiss law (AMBV), with the mid-term goal of legally taking over the deputy function. Your Profile Education: Degree in Pharmacy, Chemistry, Biology, or a comparable scientific/technical qualification. Professional Experience: Initial or several years of practical experience in Quality Assurance (QA) or Quality Management (QM), ideally within the pharmaceutical or medical device industry. Technical Knowledge: Basic knowledge or first points of contact with Swiss therapeutic products law (HMG, AMBV, GDP) and international standards (ISO 13485 / EU-MDR) are an advantage. Language Skills: Professional fluency in German, alongside good French and English skills (es