Design Quality Assurance Manager

• 25 août 2026 • 100% • Durée indéterminée • Zurich Design Quality Assurance Manager - Driving an Impact in Life-Saving Innovation Location: Zurich, Switzerland At Abbott-s Thoratec Switzerland GmbH, we develop technologies that save lives. As an integral part of Abbott's global medical devices division (more than 115,000 employees worldwide), we are leaders in implantable and extracorporeal blood pump systems using advanced magnetic levitation technology. From our Zurich site, a diverse team of 130 colleagues collaborates across development, quality, and production to provide the CentriMag system and the HeartMate 3 - supporting patients suffering from advanced heart failure across the world. Why this role is important Are you passionate about advancing innovative healthcare solutions that have a significant impact on patients' lives? As a Design Quality Assurance Manager, you will play a key role in ensuring quality, compliance, and product excellence throughout the development cycle. Working at the intersection of innovation and quality, you will collaborate closely with cross-functional teams, including R&D, Regulatory Affairs, Manufacturing, Clinical, and Project Management, to support the delivery of safe, effective, and compliant products. In this influential role, you will help shape and strengthen design control processes, risk management practices, and product development quality systems while fostering a culture of collaboration and continuous improvement. As a trusted quality partner, you will provide strategic guidance across product development activities, helping teams navigate regulatory requirements and quality expectations while enabling innovation and generating positive results for both the company and the patients we serve. What you will do • Lead Design Quality Assurance activities throughout the product development lifecycle. • Serve as the Quality representative within cross-functional product development teams. Ensure implementation and compliance with Design Control requirements. • Conduct quality planning activities for new product development projects. Provide quality oversight for design changes and product improvements. • Lead, coach, and develop Design Quality Engineers and other quality professionals. • Establish team goals, performance expectations, and development plans. Manage resource planning and project prioritization. • Promote a culture of quality, compliance, and continuous improvement. What you bring • A master's degree in science, engineering, or another technical field is required. • At least five years of relevant experience in the medical device industry. • At least 2 years of experience in team management. • In-depth knowledge of ISO 13485, international regulatory requirements for medical devices (21 CFR part 820, EU MDD/MDR), MDSAP, and other applicable regional requirements. • Proven experience in a large, regulated global organization in a leadership position. • Strong stakeholder management and communication skills. • Experience with Design for Six Sigma or Quality by Design methods will be considered a major asset. What we offer • A meaningful role contributing to life-saving technologies • A collaborative and inclusive culture where different perspectives are valued • Opportunities for growth and specialization (including becoming a cost expert) • Flexibility and autonomy in managing your work • A modern workplace in the heart of Zurich Join us We are looking for curious, motivated people who love solving problems, working together, and making an impact. If this suits you, we would be delighted to hear from you. Apply via our career site: Abbott Laboratories Careers