Clinical & Regulatory Affairs Compliance Officer - Permanent Position
Vor 2 Tagen
Responsibilities : Oversee and coordinate clinical evaluation processes for medical technology products. Ensure compliance with relevant regulatory requirements and standards. Support the development, review, and maintenance of clinical and regulatory documentation. Collaborate with cross-functional teams, including R&D, Quality Management, and Product Management. Contribute to the continuous improvement of internal expertise and processes in clinical and regulatory affairs. Monitor regulatory changes and support implementation within the organization. Assist in preparing documentation for regulatory submissions and audits. Profile : Degree in life sciences, medical technology, regulatory affairs, or a related field. Minimum 5 years experience within the Medtech industry. Experience in clinical evaluation, regulatory affairs, or compliance within the medical device industry mandatory. Strong understanding of regulatory frameworks (e.g., MDR, ISO standards). Excellent organizational skills and attention to detail. Proactive and solution-oriented mindset. Strong communication and collaboration skills. Ability to work independently and as part of a dynamic, interdisciplinary team. Votre contact pour ce poste est Leila. Avec plus de 5 ans d’expérience dans le domaine du recrutement, elle saura vous accompagner, vous conseiller et vous apporter la réponse à toutes vos questions concernant le poste. Nous ne répondrons qu’aux candidatures dont le profil correspond au descriptif demandé. #J-18808-Ljbffr
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Global Program Lead, Global Regulatory Affairs
Vor 6 Tagen
Lausanne, Schweiz Debiopharm VollzeitDescription Debiopharm is an independent biopharmaceutical company based in Switzerland with an ongoing commitment to research in oncology and bacterial infections in order to improving patient outcomes and quality of life. Our main activities include drug development, drug manufacturing and digital health investment. Debiopharm International SA aims to...
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Regulatory Affairs Specialist
Vor 6 Tagen
Lausanne, Schweiz Medtronic (Schweiz) AG VollzeitBei Medtronic kannst Du eine Karriere für Dein Leben starten. Und Dich für ein gerechtes und innovatives Gesundheitswesen einsetzen, das für alle zugänglich ist. Du wirst zielstrebig Barrieren abbauen, die Innovationen in einer stärker vernetzten und solidarischen Welt im Wege stehen. Ein Tag im Leben Medtronic is hiring a Regulatory Affairs Specialist...
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Regulatory Affairs Specialist
Vor 6 Tagen
Lausanne, Schweiz Medtronic VollzeitA Day in the Life Medtronic is hiring a Regulatory Affairs Specialist responsible for operating as an established, productive individual contributor who works independently on moderately complex projects with general supervision. In the position, you will set objectives for your own work to align with broader project goals and actively contribute to key...
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Regulatory Affairs Specialist
Vor 6 Tagen
Lausanne, Schweiz SHQ Medtronic Int. Trading Sàrl VollzeitAt Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life Medtronic is hiring a Regulatory Affairs Specialist responsible for operating as an established,...
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Regulatory Affairs Specialist
Vor 3 Tagen
Lausanne, Schweiz SHQ Medtronic Int. Trading Sàrl VollzeitAt Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.A Day in the LifeMedtronic is hiring a Regulatory Affairs Specialist responsible for operating as an established,...
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Regulatory Affairs Specialist
Vor 6 Tagen
Lausanne, Waadt, Schweiz Medtronic Vollzeit CHF 120'000 - CHF 180'000 pro JahrAt Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.A Day in the LifeMedtronic is hiring a Regulatory Affairs Specialist responsible for operating as an established,...
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Regulatory Affairs Specialist
Vor 6 Tagen
Lausanne, Schweiz Medtronic plc VollzeitRegulatory Affairs Specialist page is loaded## Regulatory Affairs Specialistlocations: Lausanne, Vaud, Switzerlandtime type: Full timeposted on: Posted Todaytime left to apply: End Date: December 19, 2025 (13 days left to apply)job requisition id: R52901At Medtronic you can begin a life-long career of exploration and innovation, while helping...
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Regulatory Affairs Specialist
vor 9 Stunden
Lausanne, Waadt, Schweiz Medtronic VollzeitAt Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.A Day in the LifeMedtronic is hiring a Regulatory Affairs Specialist responsible for operating as an established,...
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Lausanne, Schweiz SHQ Medtronic Int. Trading Sàrl VollzeitA global healthcare technology leader is seeking a Regulatory Affairs Specialist in Lausanne, Switzerland. This role involves coordinating regulatory submissions, ensuring compliance with Swiss medical device regulations, and leading product submissions. Candidates should have a Bachelor's degree in a relevant field and possess 2-5 years of medical device...
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Remote Regulatory Affairs Specialist – MedTech
Vor 6 Tagen
Lausanne, Schweiz Medtronic plc VollzeitA leading healthcare technology company based in Lausanne, Vaud, is seeking a Regulatory Affairs Specialist. This role involves regulatory submissions, compliance with the Swiss Medical Device Ordinance, and collaboration with internal stakeholders. Candidates should possess a Bachelor's degree in Life Sciences or Engineering, 2-5 years of regulatory...
