UL is a global independent safety science company with more than a century of expertise innovating safety solutions from the public adoption of electricity to new breakthroughs in areas such as sustainability, renewable energy, mobile payment security and nanotechnology. Dedicated to promoting safe living and working environments, UL helps safeguard people, products and places in important ways, facilitates trade and provides peace of mind. Our 1,000+ Standards of Safety serve as the bedrock of compliance for nearly 200 different industries. The UL mark is accepted worldwide and our reputation for public safety and helping manufacturers around the globe build safer products is unmatched. More than 11,000 employees together with representatives and business partners serve customers locally in over 100 different countries. To build up our Regulatory Medical business in Europe we are looking for: Certification decision maker (assessor and auditor) In Vitro Diagnostic Technologies.
In Vitro Diagnostics Medical Devices are some of the most regulated products in the world. In this role, you will be a part of the UL Medical Regulatory Team. Working with limited supervision, you will independently assist and support processing of manufacturer submissions to the IVD Directive 98/79/EC and, where applicable, ISO13485. Within the framework of our highly regulated Notified Body you will: