Life. Unlimited.AtSmith+Nephewwe design and manufacture technology that takes the limits off living.
We are currently searching for a Regulatory Affairs Specialist who will support with global registration and maintenance of submission of medical devices (EU – risk classes III – I) for a legal manufacturer, covering regulatory support and topics, implementation of global regulations as well as coordination within external authorities/notified body.
What will you be doing?
Ensure compliance to global regulations 2017/745, EN ISO 13485, Medical device single audit program (Australia, Brazil, Canada, Japan and US) and other relevant regulations and standards.
What will you need to be succesful?
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We're more than just a company - we're a community! Follow us on LinkedIn to see how we support and empower our employees and patients every day.
Check us out on Glassdoor for a glimpse behind the scenes and a sneak peek into You. Unlimited., life, culture, and benefits at S+N.
Explore our website and learn more about our mission, our team, and the opportunities we offer.
Stay connected by joining our Talent Community.
We're more than just a company - we're a community! Follow us on LinkedIn to see how we support and empower our employees and patients every day.
Check us out on Glassdoor for a glimpse behind the scenes and a sneak peek into You. Unlimited., life, culture, and benefits at S+N.
Explore our website and learn more about our mission, our team, and the opportunities we offer.