Regulatory Document Control Specialist
Mainstream Medical Devices, LLC
Mainstream Medical Devices, LLC is seeking a Document Control Specialist to manage controlled documents and records in compliance with ISO 13485 and FDA QMSR. You will handle DCOs, label printing, and record storage, while supporting audits and light incoming inspection of parts. The role requires meticulous attention, 1+ year in a regulated setting, and fluency in English. High school diploma required; MS Office proficiency is expected. #J-18808-Ljbffr Mainstream Medical Devices, LLC
Vacancy posted 2 days ago
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