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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