Do you bring a track record of successfully driving NGS Reagents or Diagnostic Software through IVDR submission to approval, including with notified bodies? Do you have a passion for driving innovative solutions within a regulatory framework?
If this sounds like you and you are driven by purpose, Join the SOPHiA GENETICS as an IVDR Expert for our Regulatory Affairs team as Regulatory Affairs Specialist, Manager or Senior Manager, and enable us to make a positive impact on the outcomes for cancer and rare disease patients worldwide.
Enjoy the flexibility of a hybrid work schedule allowing 2 days PW home working, collaborating closely with colleagues in either our Rolle, CH or Boston, MA corporate offices. Suitably qualified candidates can be considering remote/hybrid in EU5 or UK.
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