Denmark Job Openings
Radiometer
RA Specialist - Processes, Systems and Tools
Brønshøj
FULL TIME
November 21, 2024
Radiometer is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we’re working at the pace of change to improve patient lives with diagnostic tools that address the world’s biggest health challenges.
The RA Specialist Processes, Systems and Tools for Radiometer is responsible to drive process improvements as well as implementation of systems and tools within the Regulatory Affairs to support an efficient regulatory support to the organization and growth of the company.
This position is part of the Global Regulatory Affairs team located primarily in Copenhagen, Denmark and will an on-site position. At Radiometer, our vision is to improve global healthcare with reliable, fast, and easy patient diagnoses.
You will be a part of the Regulatory Affairs team and report to the Sr Manager, Regulatory Affairs responsible for RA Systems, Tools and Processes. The Regulatory affairs team assures that defined regulatory strategies are effectively implemented and maintained in line with changing regulatory and business needs. If you thrive in an amazing, multifunctional, leadership, fast paced, supporting role working with stakeholders across the global organization and want to work to build a world-class regulatory affairs team - read on.
In this role, you will have the opportunity to:
- Drive process improvements for RA owned processes and procedures.
- Implement systems and tools that supports the Regulatory Affairs organization towards a more efficient way of working.
- Work with key stakeholders and a cross-functional team monitoring, interpreting, and implementing new/changed legislation, standards, and guidance’s though the Regulatory Intelligence process and other processes such as MAPSS (Marketing, Advertising, Promotional, Scientific, and Sales) material.
- Minimum Master’s degree in a technical field such as chemistry, biochemistry, biology, or related required.
- Knowledge and experience in global IVD/MD regulations, quality standards such as ISO 13485, US FDA 21 Part 820, IVDR/MDR, design control, risk management, etc. required.
- Minimum 5 years of regulatory experience related to medical device/in vitro diagnostics required.
- Demonstrates excellent negotiation skills, problem-solving skills and builds consensus.
- Demonstrates effective communication skills in written and oral channels both within Regulatory and across the organization.
- Able to deliver challenging messages effectively without compromising important business relationships.
- Experience working in a complex matrix environment.
It would be a plus if you also possess previous experience in:
- Regulatory Affairs Processes, Systems and Tools
Application
We continuously assess candidates and invite them for interviews, so please don’t hesitate to write and send in the application.
We thank you for your interest. Please read our Applicant Data Privacy Notice carefully here.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.
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