Global Recall
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Merit Medical seeks a skilled regulatory affairs professional to lead post‑market surveillance and field action recalls. The role coordinates recalls, FSCAs, and regulatory reporting across functions and regions to ensure timely, compliant actions.
The ideal candidate has 3–5 years in medical device quality and regulatory affairs, with strong knowledge of FDA/EU regulations, ISO 13485, and audits. Requires cross‑functional collaboration and excellent communication skills.
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