Regulatory Affairs Manager – Medical Devices – Graubünden
NonStop Consulting
Regulatory Affairs Manager – Medical Devices
Are you an ambitious professional with a background in scientific, medical, or legal fields, seeking a new opportunity to showcase your regulatory expertise? Our client, a leading manufacturer and developer of liquid handling pipettes and robotics, is offering you a chance to join their innovative team in a new modern office space with a positive and vibrant working culture. Imagine yourself at the forefront of national and international approval procedures, making a significant impact on cutting-edge projects that drive the growth of our client.
Benefits:
– Work for a pioneering company that leads the industry in liquid handling pipettes and robotics
– Enjoy a modern and dynamic working environment that promotes creativity and collaboration
– Opportunities for professional growth and career advancement within a high-performing team
Responsibilities:
– Manage and oversee regulatory approval procedures for medical devices and laboratory equipment
– Ensure compliance with relevant standards such as ISO 9001, IEC 61010, and IEC 61326
– Collaborate with cross-functional teams to achieve regulatory milestones and product launches
Requirements:
– Academic background in scientific, medical, or legal fields
– Previous experience in regulatory affairs within the medical devices or laboratory equipment sector
– Strong proficiency in both German and English languages
About NonStop: We are NonStop, a leading provider of staffing solutions throughout Europe and now also in the US. We’re passionate about connecting talent with opportunity and work non-stop to support our clients in hiring the best talent for their teams. Feel free to pop over to our website, NonStop Consulting, for more information, to browse all our roles, or to let us know how we can help you.