Regulatory Affairs Specialist

Want to drive compliance across global markets and contribute to a mission of improving healthcare access worldwide?

Join us as a Regulatory Affairs Specialist in our new office in Copenhagen and play a key role in ensuring our medical devices meet regulatory requirements in over 85 markets.

Regulatory Affairs Assistant – track compliance in 100+ markets

Want to help build a new office in Copenhagen while supporting global compliance?

Then join us and impact the way we expand access to vital medical products across the globe.

This position enables you to dive into submissions, document tracking, and regulatory requirements across dozens of countries. You will also work closely with QA and global RA and help structure our growing impact – one detail at a time.

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!

Clinical Trial Manager – Empower progress in clinical studies

Do you thrive in a dynamic environment where your problem-solving skills and passion for optimizing workflows can truly shine?

NBCD is a world-leading CRO specializing in osteoarthritis and musculoskeletal diseases.

You will be at the forefront of driving the planning and execution: Lead the planning, implementation, management, and close-out of clinical trials, ensuring that each phase is executed with precision and care.

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.