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Lead global QA/RA strategy for a medical device company in Burlington. Ensure FDA, ISO 13485, and MDR compliance across the product lifecycle. Manage the QMS, regulatory submissions, and a team with 8-10+ years of industry experience. Drive continuous improvement in a cross-functional environment.
Location
United States , Burlington
Salary
170000.00 - 180000.00 USD / Year
Myomo
Expiration Date
Until further notice
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