Senior Quality and Regulatory Affairs Specialist – CHF 100,000 – 120,000
Early stage Medtech business
As part of the companies growth, this very exciting med tech company based in the centre of Zürich is seeking an experienced Regulatory & Quality professional to join their team.
The company has already launched the product across the EMEA region, and as part of this role you will be responsible for ensuring regulatory approval is maintained across the EMEA, as well as planning entry to the US market via FDA 510(k) submission, as well as managing the QMS to ISO 13485 & QSR standards.
My client expect to almost double in size over the next 12-18 months, so this is the best time to join a company with huge opportunity to grow and develop, whilst working in a great environment where they champion flexible working and really care about employee wellness.
This company is looking to exact a real change in this incredibly high growth sector, with a strong track record of results already, it presents a great chance to be part of something big.
If you have a passion for new medical technology, and want to help an amazing business get their products into new markets whilst ensuring its complete safety and efficacy, APPLY NOW!
Send your CV or call for a discussion about the role on +44203 854 9412
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