Preferred: One year of experience in an FDA regulated environment and/or ISO 13485 standards in the medical device industry and/or in-vitro diagnostics
Familiar with measuring equipment such as micrometer, caliper, height gauges, plug gauges
Able to lift at least 35 lbs
Strong attention to details and ability to understand and follow complex procedures
Working knowledge and experience in basic computer applications such as Microsoft Word, Excel, and Outlook
Effective and clear written and verbal communication skills in English language
Ability to conduct basic troubleshooting and problem resolution
Able to be flexible with the work schedule
Responsibilities
Perform inspections of purchased parts according to acceptance criteria using standard sampling plan
Perform First Article Inspection (FAI) of manufactured parts, electromechanical assemblies, and final assemblies
Conduct physical, mechanical, and/or electrical measurements in compliance with the company Quality System
Accurately document results of inspection/testing and maintain controlled document files, logs, and test records
Inspect cables per wiring configuration
Initiate non-conformance process and assist in resolving non-conformances
Monitor receiving inspection backlog
Process SAP transactions to segregate and disposition non-conforming product
Other duties and responsibilities in the Quality Department as assigned