Regulatory Document Control Specialist
Listed on 2026-10-18
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Quality Assurance - QA/QC
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Administrative/Clerical
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.
This is a strong position to take on the Regulatory Document Control Specialist role at Mainstream Medical Devices, LLC.
The advertised compensation is 45.000 - 65.000.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Regulatory Document Control Specialist role in the description above.
We appreciate your interest in this position.
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