Regulatory Affairs Manager – Medical Devices – Graubünden
NonStop Consulting
Regulatory Affairs Manager – Unlock Your Potential in a Global Leader
Are you a highly experienced Regulatory Affairs professional looking for a new opportunity to make a significant impact on innovative products and devices in the medical diagnostics and biotech industry? Join our client, a global leader in liquid handling robotic products, at their brand new modern offices where you can exercise your expertise in regulatory affairs. Imagine being part of a team that drives groundbreaking projects and solutions, contributing to the growth of a company that is revolutionising the industry.
Benefits:
– Work in cutting-edge modern work-spaces with state-of-the-art facilities
– Collaborate with a diverse team of experts in a dynamic and supportive environment
– Develop your skills and knowledge by working with innovative products and devices
Responsibilities:
– Lead and manage regulatory affairs activities for medical diagnostics and biotech products
– Ensure compliance with ISO standards and regulations for quality assurance and risk management
– Contribute to the development and implementation of regulatory strategies to support product registrations
Requirements:
– Scientific/medical or engineering academic background
– Several years of regulatory affairs experience in medical devices, laboratory equipment, or engineering solutions
– Strong understanding of ISO 9001, IEC 61010, and IEC 61326
– Proficiency in 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.
