Influence the future of healthcare at TÜV SÜD
TÜV SÜD was founded in 1866 to enable progress by protecting people, the environment and assets from technology related risks. Today, this purpose remains valid and embedded in our mission in servicing our eight key customer segments.
We audit and certify management systems and products for virtually all industries, ensuring your value chain complies with requirements for quality, performance, safety and IT security according to international, national and other relevant standards.
Auditors / Clinical Professionals / Product Reviewers
/ Medical Device Experts in Denmark
TÜV SÜD Product Service is among the world's first certification bodies to receive designation as a Notified Body for the new Medical Device Regulation (MDR) and is now establishing a team for the development of a new Notified Body in Denmark.
We're looking for several Medical Device Product Specialist to help certify medical products and audit manufacturers and companies, while upholding the highest standards, and enable trust in new medical technologies around the world.
Who are we looking for?
Our product specialists and auditors must have extensive knowledge that is supported by many years of experience in the most important markets. Well-founded specialist knowledge, as well as integrity, tact and neutrality, are an absolute prerequisite here.
Employees in this field of expertise are mainly responsible for the market approval and certification of new medical products, as well as for the maintenance and functional testing of operational equipment at hospitals and doctors' practices.
Candidate backgrounds could include a degree in medical technology or similar, plus relevant industry experience. If this describes you, consider Medical Devices and Healthcare for your next role!
Initially we're looking for qualified candidates to the following positions:
- Site Auditors for active and non-active medical devices.
- Product Reviewer for active and non-active medical devices within the area of neurovascular, cardiovascular, software or functional safety core competences.
- Clinical Reviewer for active and non-active medical devices within the area of neurovascular and cardiovascular devices.
More information about the qualifications, responsibilities and tasks for the different roles will be given by request. Applications should specify which role(s) are of interest.
Work location can be remotely anywhere in Scandinavia, from our office in Copenhagen, Denmark or from our office in Stockholm, Sweden.
If you are attracted by a dynamic, innovative organization with the chance to build something new, then TÜV SÜD could be the workplace for you. For more information please see: https://www.tuvsud.com/en/industries/healthcare-and-medical-devices/medical-devices-and-ivd/regulatory-strategy
For questions regarding the position, please contact Kelly Life Sciences Branch Manager Thomas Lund on +47 401 08 070, Consultant Kristina Skants on +47 406 07 346 or Consultant Ingvild Ringen on +47 988 04 308. Kelly Scientific is a recruitment agency, specialized in positions in the Life Science Industry in the Nordics.
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As an Equal Opportunities employer, we welcome applications from all suitably qualified persons regardless of their race, sex, disability, religion/belief, sexual orientation or age.