Senior QARA Specialist for Class III MedTech Device

A leading Swiss research institution is seeking a Quality & Regulatory Affairs Specialist (QARA) to facilitate the regulatory strategy for Class III medical devices. This role is central to bridging engineering, quality assurance, and regulatory partners, ensuring compliance in bringing innovative surgical technologies to the clinic. Candidates should...

Quality & Regulatory Affairs Specialist (QARA) – Class III Medical Device At Veltist – a Wyss Zurich project – we are reshaping post-operative care through our platform technology AnastoSeal, enabling the next generation of implantable biomaterials for sealing, healing, and integration with human tissue. Veltist is a pioneering MedTech spin-off from...

Quality & Regulatory Affairs Specialist (QARA) – Class III Medical Device 80%-100%, Zurich, fixed-term At Veltist – a Wyss Zurich project – we are reshaping post-operative care through our platform technology AnastoSeal, enabling the next generation of implantable biomaterials for sealing, healing, and integration with human tissue. Veltist is a...

A leading MedTech recruiting company is seeking a Post-Market Surveillance Specialist in Zurich, Switzerland. This role involves managing complaints, vigilance reporting, and improving quality systems within a Class III medical device company. Candidates should have at least 3 years' experience in the medical device industry and excellent communication...

Senior Talent Partner | Medical Affairs | Clinical Affairs | Regulatory Affairs | Quality 🔎 Role: Post-Market Surveillance (PMS) Specialist 🔹 The Role & Company Join a well established, growing and dynamic company designing, developing and producing a Class III active implantable medical device that changes the lives of patients. This is a great...

A leading MedTech recruiter is seeking a V&V Manager to enhance quality systems for a Class III medical device. This role entails leadership in validation and verification activities, and it reports to the VP of QA. You're expected to have 5+ years in the medical device sector, specifically under ISO 13485 and FDA compliance, and excellent English and German...

Senior Talent Partner | Medical Affairs | Clinical Affairs | Regulatory Affairs | Quality 🔎 Role: Post-Market Surveillance (PMS) Specialist Role & Company Join a well established, growing and dynamic company designing, developing and producing a Class III active implantable medical device that changes the lives of patients. This is a great opportunity to...

A medical device company in Zürich is looking for a Quality Assurance Specialist to support audits, inspections, and quality training. The ideal candidate has a minimum of 3 years of experience in the medical device industry and excels in a certified ISO 13485 environment. Excellent communication skills in English are required, and German would be a bonus....

A leading medical device company in Zürich is seeking a Quality Assurance Specialist to support audits and ensure compliance in a certified environment. The ideal candidate has at least 3 years of experience in Quality Assurance within the medical device industry. This role involves collaboration with the production line and senior leadership, along with a...

Founded in 2021, Nanoflex Robotics was spun out of Switzerland's leading research university, ETH Zurich. Today, we are a medical device company specializing in the development of telerobotic solutions to treat a range of critical endovascular diseases. Recognized as the top Medtech start-up in Switzerland for the last two years, we are driven by our mission...