Dexian seeks a Vigilance Writer for a 3+ month engagement, with work from home from Acton, MA. The role develops QA methodologies for post-market vigilance and regulatory reporting in the medical device field.
You will author and review vigilance reports, code complaints, support audits, and collaborate with engineering, laboratories, and clinical staff to ensure timely regulatory submissions and CAPA processes.
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📌 Global Medical Device Vigilance Writer (Remote) (Alberta)
🏢 Dexian
📍 Alberta
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