- Clinical Research Associate
- Success Manager
- Manager
- Engineer
- Project Manager
- Senior Clinical Research Associate
- Principal Clinical Research Associate
- Maintenance Supervisor
- Working Student
- Software Engineer
- Business Development Manager
- Quality Assurance Engineer
- Engineering Project Manager
- Director
- Compliance Manager
Join Clario, part of Thermo Fisher Scientific, as Director, Regulatory Affairs (f/m/d) and play a critical role in ensuring that innovative clinical trial technologies meet global regulatory standards - helping bring life-changing therapies to patients faster. In this
Drive the future of stress testing in a dynamic European banking environment. As a Stress Test Lead, you will play a pivotal role in safeguarding the institution’s resilience, working closely with senior stakeholders and cross-functional teams.
At Elanco (NYSE: ELAN) – it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and
JOB DESCRIPTION: About Abbott Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. In Germany, Abbott has more than
Job Description Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance partnering with external regulatory agencies. We are on the leading-edge of healthcare breakthroughs that help
Thank you for your interest in joining Solventum. Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. At Solventum, people
Position Summary: The Director, CDx Regulatory Consultant will be responsible for applying deep expertise in companion diagnostic regulatory strategy, IVD development, quality system expectations, and global marketing authorization pathways to advise pharmaceutical, biotechnology, and diagnostic clients on the
Job title: Principle Regulatory Affairs Specialist – DACH Department: Regulatory Affairs Location: Darmstadt, Germany Working hours: Full time A brighter future awaits you CooperVision is one of the world’s leading manufacturers of soft contact lenses with a presence
Position Summary: The Director, CDx Regulatory Consultant will be responsible for applying deep expertise in companion diagnostic regulatory strategy, IVD development, quality system expectations, and global marketing authorization pathways to advise pharmaceutical, biotechnology, and diagnostic clients on the
Regulatory Affairs Support Manager (m/w/d) North America Developing surgical innovations is our passion. Our employees expertise, motivation, and commitment are crucial to this. That is why we always look for people who set goals for themselves, develop
At eBay, were more than a global ecommerce leader — we’re changing the way the world shops and sells. Our platform empowers millions of buyers and sellers in more than 190 markets around the world. We’re
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It
YOUR CONTRIBUTION As a Regional Regulatory Affairs Manager (m/f/d), you will provide regional regulatory support for the strategic development, approval, and life cycle management of drugs, ensuring compliance with regulatory and legal requirements in the region APACMEA. This will
YOUR CONTRIBUTION As a Regional Regulatory Affairs Manager (m/f/d), you will provide regional regulatory support for the strategic development, approval, and life cycle management of drugs, ensuring compliance with regulatory and legal requirements in the region EU/UK/CH. This will
We are the people who give possibilities purpose BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it’s no small feat. It takes
Job Description Who will you be working with? As a Technical Documentation Specialist - Railway Display and Audio Systems & Device Engineering at Wabtec, you will be part of a highly collaborative engineering environment focused on railway
Head of Tax Strategy About the team SumUp’s tax team is evolving, and this role will play a critical part in shaping its next chapter. Reporting to the Global Head of Tax, you’ll lead the execution
The Position Join us as a Senior Scientist in Computational Pathology and help shape the future of non-clinical safety science through cutting-edge AI technologies. In this role, you will combine deep scientific expertise with advanced computational