Quality Inspector I

Role: Quality Inspector I responsible for performing quality assurance inspections of purchased components, sub-assemblies, and finished products in a medical device manufacturing setting. Objectives include ensuring compliance with FDA regulations, ISO standards, and company policies. Core duties involve first article, incoming, and in-process inspections using varied measurement tools, interpreting drawings and specifications, maintaining inspection records, and supporting validation and rework activities. Responsibilities also encompass training new associates, conducting quality reviews, and working in clean room environments. Qualifications: High School Diploma, QA experience in medical devices preferred, knowledge of ISO 13485, 21 CFR 820, and cGMP desirable. Skills include organizational aptitude, problem-solving, attention to detail, and ability to work independently and in cross-functional teams. High-Value Details: Role involves inspection in sterile clean room conditions, requires visual acuity, and may involve lifting up to 50 lbs. Shift is 4 days/week, 10 hours per day, with some physical movement around manufacturing areas. Compensation ranges from $19.19 to $25.43/hour, with potential benefits and bonus eligibility. This position is structured for candidates capable of adhering to strict quality and regulatory standards in a regulated manufacturing environment.