Principal Specialist, Quality Management Systems
12-month Contract
On-site Cary, IL
Must be able to work on a W2
We are seeking a Principal Specialist, Quality Management Systems with strong knowledge of US and International Medical Device Regulations, including MDSAP, and experience with US 510(k) and EU Class II devices. The role involves ensuring compliance, managing quality systems, supporting cross-functional teams, driving projects, and providing actionable insights from data. Excellent communication, problem-solving, and technical writing skills are required.
Responsibilities:
Qualifications:
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