The QC Associate supports raw material, in-process, and finished goods testing in an ISO 13485/cGMP environment. This role performs routine inspections, documents results, maintains lab equipment, and ensures compliance with quality and safety standards. The individual will work with complex systems, support investigations (OOS/non-conformance), maintain inspection-ready labs, and generate QC documentation for Device History Records.
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Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree