QA Coordinator

Location: Greenville, SC. Duration: 5+ months.

Responsibilities

• 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

Requirements

• Product Inspection
• Incoming Material Inspection
• Vision Inspection
• Keyence
• Non-Conforming Material Reports (NCMRs)
• High School diploma or equivalent
• 5+ years of Quality Control experience in the biomedical industry