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Job description
Abbott is seeking a Postmarket Surveillance Analyst to manage complaint investigations and product evaluations for a broad range of medical devices. The role involves regulatory reporting, data entry, and coordination with Regulatory, Quality Engineering, and other teams.
You will perform product evaluations, prepare technical findings, and maintain compliant documentation while supporting QMS/EMS activities and ensuring timely regulatory filings.
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Worksite address
burlington, MA, 01805, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.