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5 jobannoncer
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Regulatory Affairs & Safety Manager
Are you known for being well-organized and structured with a keen eye for details? Do you thrive on working independently and taking accountability for your responsibilities? Are you passionate about making a difference in a global research organization dedicated to providing first-class clinical research?
You will lead the planning and execution of the Regulatory Affairs & Safety activities and collaborate closely with the Clinical Trial Management team and the Medical Affairs team.

Supplier Quality Engineer
We are looking for a Senior Supplier Quality Engineer to join our team. The main responsibilities include ensuring compliance with various Regulations and Standards, leading Supplier Quality Compliance Projects, developing Partner Quality Agreements, managing high visibility SCARs, and conducting key Supplier Audits.
If you have expertise in Supplier Quality and a passion for process improvement, we want to hear from you!


Principal Specialist - Design Control and Risk Management
Are you passionate about ensuring the highest standards of quality in medical devices? Do you thrive in a collaborative environment where your expertise can make a real difference?
As the Principal Specialist for Design Control and Risk Management, you will be responsible for the continuous support and development of our global quality processes across multiple business areas, including Ostomy Care, Chronic Care, Wound & Skin Care, Continence Care, Consumer Business, and Interventional Urology.


Clinical Research Associate (CRA) – Shape the Future of Drug Development
Are you passionate about clinical research and eager to make a significant impact in the world of drug development?
We are seeking a dedicated Clinical Research Associate (CRA) to join our dynamic team at the forefront of international drug development research. Join us in an environment fueled by dedication and inspired by our core values: "Team up, Take on, and Try out."
Here, you'll have the chance to make a significant difference while expanding your skillset.
Manager/Director within Regulatory CMC, Global Regulatory Affairs
Are you experienced within the Regulatory CMC area taking a strategic perspective in handling CMC documentation for pharmaceutical products?