Are you a current Elekta employee? Please click here to apply through our internal career site Find Jobs - Elekta. Want to join a team with a mission to improve and save lives? We continually look for
Do you want your voice heard and your actions to count? Discover your opportunity with Mitsubishi UFJ Financial Group (MUFG), one of the world’s leading financial groups. Across the globe, we’re 150,000 colleagues, striving to make
WHO ARE WE? ROPU MIDI is a Regional Operating Unit that covers all local Human Pharma and Animal Health Operating Units across Belgium, Denmark, Norway, Finland, Greece, Portugal, Sweden, and The Netherlands. MIDI has a multicultural
Job TitleHead of Clinical Affairs Personal Health Job Description Job Responsibilities Provide clinical and medical thought leadership to inform strategic decisions, product roadmaps, solution innovation, and market expansion. Build and strengthen critical business capabilities across Medical Affairs, Medical
WHO ARE WE? ROPU MIDI is a Regional Operating Unit that covers all local Human Pharma and Animal Health Operating Units across Belgium, Denmark, Norway, Finland, Greece, Portugal, Sweden, and The Netherlands. MIDI has a multicultural
Job Description As a Senior Government Affairs Analyst, you will serve as a trusted advisor to the business, specializing in EU legislation regarding food, packaging and consumer products. You will bridge the gap between policy and commercial
Job Description As a Senior Government Affairs Analyst, you will serve as a trusted advisor to the business, specializing in EU legislation regarding food, packaging and consumer products. You will bridge the gap between policy and commercial
About myTomorrows myTomorrows is a global health tech company dedicated to breaking down barriers for patients seeking treatment options. We strive to enable earlier and better treatment access by bridging the gap between those searching for
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description As part of Thermo Fisher Scientific’s mission to enable our customers to make the world healthier, cleaner and safer, the Manager, Regulatory Affairs – EMEA is responsible for leading regulatory
Job Description Make your mark on global animal health and step into a role where your regulatory expertise drives innovation, ensures compliance, and brings impactful solutions to markets worldwide. Join our team in Boxmeer as a:
Location: Amsterdam, the Netherlands Job type: Full time, Permanent About the job: Join our dynamic team as a full-time Regulatory Affairs (RA) Manager in the Netherlands Dutch team! Under the guidance of Layla Fitoury, our Head of
Public Affairs Manager & Patient Engagement Lead Location: Amsterdam Permanent role *When applying in addition to a CV please include a Cover Letter. About the job The Public Affairs Department in Amsterdam engages with external stakeholders to strategically
Regulatory Affairs Specialist Location: Oss The Regulatory Affairs (RA) Specialist within the Development & Manufacturing department, ADS Licensing, is responsible for the preparation, review, and maintenance of high-quality regulatory submission documents describing the chemistry, manufacturing, and controls (CMC)
Development Manager II, Large Molecules D&M ADS Licensing Location: Oss The Development Manager leads and coordinates the end-to-end development of GlycoConnect and other components, from early-stage research through process scale-up and commercial manufacturing. Independently manage technology
IntroductionWe are looking for a Legal Counsel to join our European Legal team in Eindhoven. In the role of Legal Counsel, you act as a trusted legal business partner supporting our Benelux Business Units and the
SUBJECT MATTER EXPERT – EU PPWR & Sustainable Packaging Compliance Introduction Shape the Future of Packaging: Help FoodChain ID’s Clients Navigate the EU’s Landmark PPWR Regulation. What Youll Do Advise customers (brand owners, converters, packaging manufacturers)
We Make Life More Rewarding and Dignified Location: Roosendaal Department: Summary The Global Manager, Distribution & Sterilization Quality is responsible for providing end‑to‑end quality oversight of global distribution centers, third‑party logistics providers (3PLs), and post‑sterilization
Overview Regional Distribution Compliance Specialist (40 hours/ week) Spurkterweg 16 Venray 5804 AP Netherlands About the role: As a Regional Distribution Compliance Specialist, you will be responsible for creating and maintaining a strong compliance structure across
R&D Intern – Scientific Messaging Location: Wageningen, Netherlands Hybrid: 3 days per week in the office Start date: September 2026 Duration: 6 months About the role We are seeking a motivated and detail-oriented and science-driven R&D
https://www.dekra.nl/nl/home/ solliciteren What will your role involve The Medical division is a leading and fast-growing Notified Body within the Medical Device Industry. Consequently, we are consistently looking for medical auditors or technical file reviewers. Dealing with