Sonova is seeking a Regulatory Systems Analyst Co-op to support regulatory activities for medical devices in global markets. You’ll assist with regulatory documentation, product registrations and cross-functional teamwork during product development and market clearance.
The role emphasizes learning in regulatory affairs, quality assurance, and understanding international regulatory landscapes in Canada, the US, and EU markets, with onsite work in Kitchener, Ontario and occasional remote days.
This opportunity is for the Regulatory Systems Analyst Co-op (Med Devices) role at Sonova Group.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Regulatory Systems Analyst Co-op (Med Devices) role in the description above.
We appreciate your interest in this position.
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