QA Coordinator

Location: Greenville, SC

Duration: 5 months

Duties: Conduct thorough product inspections according to Standard Operating Procedures (SOPs) to verify compliance with design specifications Perform incoming material inspections using vision inspection systems such as Keyence Generate Non-Conforming Material Reports (NCMRs) for products or materials that fail to meet specifications Create, maintain, and organize inspection records and retain samples according to quality protocols Proactively identify and recommend process improvements through critical thinking and problem-solving Verify test equipment and tools are properly calibrated according to established calibration programs Perform additional quality-related activities as assigned by management

Skills: Experience with Metrology Inspection Equipment Experience with SAP or similar ERP systems Knowledge of ISO 9001:2015 / ISO13485:2016, 21 CFR 820's QMS Proficiency with basic inspection tools (Calipers, Gauges, etc.) Strong problem-solving, critical thinking, and organizational skills Excellent written and verbal communication abilities Proficient in Microsoft Excel and Word Ability to work collaboratively in a team environment Physical ability to lift and/or move up to 50lbs

Required: Product Inspection Incoming Material Inspection Vision Inspection Keyence Non-Conforming Material Reports (NCMRs)

Education: High School diploma or equivalent 5 years of Quality Control experience in the biomedical industry.