At Applied Medical, we are committed to make a meaningful, positive difference, each and every day. Within our European headquarters in Amersfoort (NL), we develop, manufacture, and support the implementation of our advanced medical devices across Europe and the MENA region. Applied’s team members enjoy working in an environmentally friendly and international environment, in which people of diverse backgrounds are valued, challenged, and acknowledged. We support our team members by giving them opportunities for ongoing learning and education, possibilities to take part in community volunteering activities, and a variety of onsite exercise classes and health activities.
If you are passionate about working in an organization that allows you to make decisions based upon what is right for the patient, customer, community, and environment, Applied Medical is the place for you.
As Regulatory Affairs Manager you provide guidance regarding compliance with European regulations and lead the Regulatory Team. You are the crucial link between Applied Medical, our medical device products and the regulatory authorities. In this dynamic position within our vertically integrated company, you will contribute to MDD compliance and contribute to MDR readiness. The advice the Regulatory Affairs team provides coordinates the approval and post-market surveillance of our products.
As Manager Regulatory affairs you will report to the VP Operations.
Within Applied Medical this position has the internal job title of Regulatory Affairs Manager.
Are you an individual who thrives in a fast-paced, challenging, and professional, yet casual business environment? We are looking forward to receiving your application. For more information regarding our hiring process, click here.