Merit Medical Systems in Utah is looking for a Platform Principal Regulatory Affairs Specialist to drive regulatory strategies for medical device projects. The ideal candidate will have over 15 years of experience in regulatory submissions, with a strong understanding of medical device regulations like ISO 13485.
This role involves collaboration with various stakeholders to ensure compliance with global regulatory processes while representing the company to regulatory authorities. The position offers a full-time schedule with benefits and opportunities for continuous improvement within the team.
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