Devices Development Quality Lead

Location: Bulle, SwitzerlandActivity rate: 100%Contract: temporary contractStart date: 02.06.2025End date: 30.12.2025UCB, one of Switzerland's Best Employers, is an internationally active biopharmaceutical company specialising in the therapeutic areas of neurological disorders and immunology. The Bulle site is home to the company's Swiss sales subsidiary and...

At Randstad, we are seeking a talented Medical Device Quality Lead to join our team in Switzerland. As a key member of our quality assurance team, you will be responsible for ensuring the highest standards of quality and regulatory compliance for our medical devices.The ideal candidate will have a strong background in design control and quality management...

Job DescriptionThe Bulle site is home to UCB's Swiss sales subsidiary and primarily a biotechnological and chemical production platform for the manufacture and distribution of pharmaceutical specialities.We are seeking a Devices Development Quality Lead to drive QA activities for Medical Devices and Combination Products. In this global role, you will ensure...

Key ResponsibilitiesAs a Devices Development Quality Lead, you will be responsible for providing expert QA support for vendors in design, development, testing, and manufacturing of Medical Devices and Combination Products.You will also oversee Design & Development activities, including Validation/Verification, risk management, and regulatory...

About the RoleThis position reports to the Head of Pipeline Drug Delivery Devices Quality and is responsible for driving QA activities for Medical Devices and Combination Products.You will collaborate with key vendors and internal teams to ensure compliance with regulations and standards.Your key responsibilities include:Reviewing and approving key...

As a Medical Device Regulatory Scientist, you will be part of a dynamic and growing team dedicated to improving patient outcomes.Your key responsibilities will include:Planning and executing regulatory activities for medical devices and combinations products.Preparing and maintaining Technical Documentation Files, ensuring compliance with regulatory...

We are looking for a skilled Device Development QA Specialist to drive QA activities for Medical Devices and Combination Products. In this role, you will ensure compliance with regulations and standards while collaborating with key vendors and internal teams.Your key responsibilities will include providing expert QA support for vendors in design,...

The successful candidate for the Quality Assurance Manager for Medical Devices role will have a strong background in quality management and regulatory compliance. They will be responsible for ensuring that all medical devices meet the required standards and regulations.In this role, you will be working closely with vendors and internal teams to ensure...

Groupe de conseil international fondé en 2019, Ekkiden anime un écosystème de consultants passionnés et engagés qui mènent des projets de transformation organisationnelle, opérationnelle et technologique dans l'IT/Digital, l'Industrie/R&D et la sustainability, chez les grands comptes et PME, en France, Suisse, Espagne et Allemagne.Le rôle :Vous serez...

**Make your mark for patients** We are looking for a **QA System Lead **at **80% working time, **who is **autonomous, proactive, team player and who has a well-developed sense of discretion** and commitment to join us in our **HSE & Quality Culture &Compliance **department, based in our **site** in **Bulle, Switzerland.** **About the role** As a QA System...

**Make your mark for patients** We are looking for a **QA System Lead **at **80% working time, **who is **autonomous, proactive, team player and who has a well-developed sense of discretion** and commitment to join us in our **HSE & Quality Culture &Compliance **department, based in our **site** in **Bulle, Switzerland.** **About the role** As a QA System...

Key ResponsibilitiesWe are seeking a Senior Development Team Leader to join our team at Liebherr Machines Bulle SA. The ideal candidate will possess a strong background in combustion engine development and have at least 10 years of experience in coordinating project teams within a matrix organization.The successful candidate will be responsible for the...

Company OverviewNespresso HQ is a global leader in the coffee industry, dedicated to delivering high-quality products and exceptional customer experiences. Our company culture values innovation, sustainability, and social responsibility.Job DescriptionWe are seeking a highly skilled Senior Quality & Analytics Specialist to join our team at Nespresso HQ. The...

Job DescriptionWe are seeking an experienced Quality Systems Professional to lead our Bio Manufacturing Science and Technology (MSAT) team. As a key member of our Global Quality organization, you will be responsible for providing expert guidance on quality systems and processes to ensure regulatory compliance and product quality.Main...

We are looking for a Medical Device Regulatory Scientist to join us in our Global Regulatory Affairs team, to be based in any of our Brussels (Belgium), Bulle (Switzerland) or Slough (UK) offices.The Medical Device Regulatory Scientist is responsible for regulatory activities for marketed and development medical devices and combinations products within the...

About UsNespresso HQ is committed to elevating the world of coffee and driving positive change through our products and services.Job SummaryWe are seeking a Senior Quality & Analytics Specialist to join our team at Nespresso HQ. This role involves ensuring the proficiency and optimal functioning of HQ Quality Methods implementation and appropriate validated...

Make your mark for patients We are looking for a Medical Device Regulatory Scientist to join us in our Global Regulatory Affairs team, to be based in any of our Brussels (Belgium), Bulle (Switzerland) or Slough (UK) offices The Medical Device Regulatory Scientist is responsible for regulatory activities for marketed and development medical devices...

Our CultureNespresso HQ has a culture that values innovation, sustainability, and social responsibility.Job RequirementsTo be considered for this role, you will need:Background in Biology, Chemistry, Material Science or relevant fieldStrong Laboratory experience in performing analyses in the specific area of competenceSolid experience in methods development...

**Make your mark for patients.** We’re here because we want to build the future and transform patients’ lives for the better. At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care...

Role SummaryThe Bio Manufacturing Science and Technology (MSAT) Quality Lead will be responsible for leading our MSAT team and ensuring the delivery of high-quality products while maintaining regulatory compliance. This is an exciting opportunity to join our Global Quality organization and contribute to the development of our quality systems and...