Quality Inspector

Essential duties and responsibilities include: Conducts incoming acceptance activities and releases components to production. Evaluates and releases finished product. Reviews Material History Records and Device History Records for completeness, accuracy and Regulatory Compliance and Control. Writes Standard Operating Procedures as requested by the Team Leader. Identifies process/product nonconformities and ensures short term corrective actions are developed and implemented. Performs scheduled calibrations on testing and measuring instruments. Evaluates in-process forms and equipment parameters for internal audits and assist in improving process and production. Assists in training hourly manufacturing personnel in the requirements of the quality system. Informs Team Leader if corrective actions are needed in production areas. Works mandatory overtime as required.

Education: High School Diploma/GED Required

Experience: 2 – 3 years related experience. Experience in Science/Chemistry or Quality Control preferred not required Experience in medical device manufacturing preferred. (helpful) Additionally: Good written, verbal, interpersonal, general math, chemistry, and computer skills. Ability to troubleshoot and conduct to pay close attention to detail. Ability to visually inspect and handle small parts with calipers, micrometers and other measuring tools Ability to perform repetitive and routine inspections while maintaining high level of quality and to perform and prioritize multiple duties and tasks without direct and constant supervision. Ability to perform light lifting. Ability to work overtime as workload dictates.