Sea Medical Device Regulatory Affairs Specialist

A global medical device company is seeking a Regulatory Affairs Specialist for the SEA market in Queenstown, New Zealand.

The role involves regulatory submissions, compliance management, and cross-functional collaboration.

Ideal candidates will have a degree in Engineering or Science and 2-3 years of regulatory affairs experience in medical devices.

Excellent communication skills and knowledge of SEA regulations are essential.

This is a full-time role offering competitive compensation.

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