Aktuelle Jobs im Zusammenhang mit Head of Quality and Regulatory Affairs - Lausanne - Xsensio
-
Director of Regulatory Affairs
vor 13 Stunden
Lausanne, Waadt, Schweiz elemed VollzeitSenior Talent Partner | Medical Affairs | Clinical Affairs | Regulatory Affairs | QualityRole: Executive Director / VP Divisional Regulatory AffairsThe company:This is an exciting position to join a world leader at the forefront of healthcare innovation. With over 50,000 employees worldwide, the Regulatory Senior Director will be THE leader for all...
-
Regulatory Affairs Expert
vor 1 Woche
Lausanne, Waadt, Schweiz Voisinconsulting VollzeitJob DescriptionWe are seeking an experienced Regulatory Affairs Expert to join our team at Voisinconsulting. The ideal candidate will have a strong background in Clinical Trial Submissions and regulatory affairs, with 4+ years of experience in managing submission packages from start to finish.This role involves identifying and coordinating international,...
-
Head of Quality
vor 2 Wochen
Lausanne, Schweiz LHH Vollzeit**Head of Quality - Medical devices - Vaud** For one of our clients, a medical devices company based in Canton de Vaud, LHH Recruitment Solutions is recruiting a **Head of Quality in Medical Devices**. The Head of Quality will be responsible to manage **Quality Assurance, Quality Control** and **Quality **support to manufacturing, Validation teams and...
-
Quality and Regulatory Manager
Vor 3 Tagen
Lausanne, Waadt, Schweiz Distalmotion SA VollzeitOverview:The Regulatory Affairs Specialist will be responsible for leading regulatory projects, developing and implementing strategic plans, and ensuring compliance with European and international market requirements.This role involves collaborating with cross-functional teams, assessing changes to existing products or processes, and evaluating their impact...
-
Head of Medical Affairs
vor 2 Wochen
Lausanne, Schweiz Debiopharm VollzeitDescription Debiopharm is an independent biopharmaceutical company based in Switzerland with an ongoing commitment to research in oncology and infectious diseases in order to improve patient outcomes and quality of life. Our main activities include drug development, drug manufacturing and digital health investment. Debiopharm International SA aims to...
-
Paralegal Professional
vor 22 Stunden
Lausanne, Waadt, Schweiz Wyss Center for Bio and Neuroengineering VollzeitWe are seeking a highly skilled and experienced Paralegal Professional - Regulatory Affairs to join our team at the Wyss Center for Bio and Neuroengineering.About the Position:This is an exciting opportunity for a motivated and detail-oriented individual to play a key role in the development of regulatory affairs within the life sciences sector. The...
-
Regulatory Affairs Professional
vor 22 Stunden
Lausanne, Waadt, Schweiz The Biopôle VollzeitAbout the RoleThe Biopôle is seeking a talented Regulatory Affairs Professional to join our team. As a key member of our quality department, you will be responsible for ensuring compliance with regulatory requirements and industry standards.Key Responsibilities:Regulatory Compliance: Ensure compliance with relevant regulations, standards, and industry...
-
Senior Regulatory Affairs Specialist
vor 4 Wochen
Lausanne, Schweiz Intuitive Surgical VollzeitFor one of our clients, a global leader in biotechnology based between Geneva and Lausanne, we are looking for a Regulatory Affairs Officer (M / F).As part of a 9-month project and the launch of a product in the biotechnology market, we are looking for a candidate available immediately (within 1 month maximum). There are possibilities to continue on a...
-
Regulatory Affairs Specialist
vor 3 Wochen
Lausanne, Waadt, Schweiz Distalmotion SA VollzeitJoin Us in Empowering Access to Robotic SurgeryAt Distalmotion, we believe patients deserve best-in-class minimally invasive care. Our mission is to empower access to the benefits of robotic surgery. The DEXTER Robotic Surgery System uniquely simplifies operations so more surgeons, in more ORs, can provide the benefits of robotics to more patients.Whether in...
-
Regulatory Affairs Specialist
vor 3 Wochen
Lausanne, Waadt, Schweiz MedTech Innovator VollzeitAbout usAt Distalmotion, we believe that every patient undergoing minimal invasive surgery should benefit from the best of surgical expertise and robotic technology. This is the vision that made us create Dexter, the world's first and only on-demand robotic surgery system. Thanks to Dexter, surgeons have never been closer to their patients while benefiting...
-
Senior Regulatory Affairs Specialist
vor 3 Wochen
Lausanne, Waadt, Schweiz Intuitive VollzeitAt Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints.As a pioneer and market leader in robotic-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a...
-
Senior Regulatory Affairs Specialist
Vor 4 Tagen
Lausanne, Waadt, Schweiz Intuitive Surgical VollzeitAt Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints.As a pioneer and market leader in robotic-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a...
-
Regulatory Affairs Expert
vor 11 Stunden
Lausanne, Waadt, Schweiz elemed VollzeitThis is an exciting opportunity to lead the regulatory affairs division at a world-leading healthcare company.As Executive Director, Regulatory Affairs, you will be responsible for formulating the regulatory strategy for the division, developing departmental budgets, and representing the RA department in company projects.You will harmonize regulatory...
-
Regulatory Affairs Expert
Vor 3 Tagen
Lausanne, Waadt, Schweiz Distalmotion SA VollzeitAbout the Role:We're seeking a highly skilled Regulatory Affairs Specialist to lead regulatory projects and develop strategic plans for meeting European and international market requirements.This role requires excellent communication and collaboration skills, as well as strong analytical and problem-solving abilities. The successful candidate will work...
-
Global Regulatory Affairs Manager
vor 1 Woche
Lausanne, Schweiz Debiopharm VollzeitDescription Debiopharm is an independent biopharmaceutical company based in Switzerland with an ongoing commitment to research in oncology and infectious diseases in order to improve patient outcomes and quality of life. Our main activities include drug development, drug manufacturing and digital health investment. Debiopharm International SA aims to...
-
Senior Regulatory Affairs Specialist
Vor 5 Tagen
Lausanne, Waadt, Schweiz Intuitive Surgical VollzeitAt Intuitive Surgical, we're committed to fostering an inclusive and diverse team that drives innovation and excellence in the field of robotic-assisted surgery. As a Senior Regulatory Affairs Specialist, you'll play a critical role in ensuring our products and operations comply with European environmental regulations and industry standards.This challenging...
-
Functional Business Relationship Manager Quality
vor 4 Wochen
Lausanne, Schweiz Galderma VollzeitWith a unique legacy in dermatology as well as decades of cutting-edge innovation, Galderma is the leading company solely dedicated to skin and advancing the future of dermatology. We look for people who focus on getting results, embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all,...
-
Compliance and Quality Assurance Manager
vor 22 Stunden
Lausanne, Waadt, Schweiz Michael Page International (Switzerland) SA VollzeitJob DescriptionWe are seeking an experienced Regulatory Affairs Engineer to join our team. The successful candidate will have:A strong technical background in Life Sciences, with a solid understanding of regulatory frameworks.Proven experience in a regulatory role, with a track record of success in compliance and quality assurance.Excellent communication...
-
Global Quality Compliance Manager
vor 4 Wochen
Lausanne, Schweiz LHH VollzeitFor one of our clients, an international company in Canton de Vaud, we are looking for a** Global Quality Compliance Manager** Missions: - Collaborate to ensure Compliance of the Global QMS to the most current version of applicable International Medical Product, Regulations and Standards through effective implementation, training, and monitoring. - Support...
-
Global Quality Compliance Manager
vor 18 Stunden
Lausanne, Schweiz LHH VollzeitFor one of our clients, an international company in Canton de Vaud, we are looking for a** Global Quality Compliance Manager** Missions: - Collaborate to ensure Compliance of the Global QMS to the most current version of applicable International Medical Product, Regulations and Standards through effective implementation, training, and monitoring. - Support...
Head of Quality and Regulatory Affairs
vor 1 Monat
Xsensio is a Swiss start-up company developing the Lab-on-SkinTM sensing platform to sense in real-time biochemical information at the surface of the skin, providing unprecedented real-time information about our health and wellness, in a simple and mínimally invasive way.
To strengthen our team (EPFL Innovation Park, Lausanne, Switzerland), we are looking for a **Head of Quality and Regulatory Affairs** (XS21-B-03).**
**Roles and Responsibilities**:
As Head of Quality and Regulatory Affairs in a fast-paced cross-functional team, you will oversee all aspects related to quality and regulatory affairs to plan for the market launch of medical devices. You will play a hands-on role on the team, and focus on:
- Developing a regulatory strategy for our product pipeline in conjunction with the company management and the R&D and product development teams, and overseeing its implementation on multiple markets.
- Selecting, implementing and maintaining quality system processes, in compliance with Quality System Regulation. Managing all aspects of regulatory compliance with the FDA, Swiss Medic and EU notified bodies.
- Organizing clinical studies activities together with scientific experts, in accordance with ethics regulations.
**Requirements**:
- Master’s or PhD degree in bioengineering, medicine or life sciences, with 5+ years of experience in a similar managerial position in the medical device industry (preferably with class II devices).
- Experience successfully implementing a medical quality system.
- Experience interacting with Regulatory Authorities and Notified Bodies, with a detailed understanding of the EU, Swiss and USA medical device regulations.
- Experience successfully launching a medical device on the market a plus.
- Experience in project management.
- Strong interpersonal skills, ability to work independently and take initiatives. Excellent verbal and written communication skills.
- Fluency in English; proficiency in French a plus.
- Swiss or EU/EFTA work permit.
Xsensio is an equal opportunity employer: we celebrate diversity and are committed to creating an inclusive environment for all employees.
No recruiters or agencies please.
