Regulatory Affairs Specialist
CHE - Zug/HOonsitemid
Posted today · via Workday
About this role
Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living . We are currently searching for a Regulatory Affairs Specialist who will support with g lobal 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? Handling and maintenance of regulatory (re-)submissions in EU according to Medical Device Regulation 2017/745 (MDR) of Smith&Nephew Orthopaedics AG products main contact to the notified body .…
What we'd score you on
reqspace match rubricFive dimensions, recruiter-grade. Upload your resume and we'll generate a written explanation of where you fit and where the gaps are.
1
Skills match
We compare your skills against the role requirements.
2
Level fit
This role is mid-level. We check your trajectory against it.
3
Domain experience
Your work in the role's domain matters more than your years total. We weight recent and direct experience.
4
Recency
A skill you used last quarter weighs more than one from five years ago. We grade on recency, not lifetime.
5
Location fit
This role is based in CHE - Zug/HO. We weight your proximity and willingness to relocate.
Score yourself on this role.
Free · no card · written explanation included
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