Job Summary
The purpose of the Inspector–I role is to perform visual inspections in order to identify conforming and nonconforming product within the Tegra Medical location.
Role and Responsibilities
Responsible for QC Visual Inspections of finished products required in accordance with ISO 13485.
Accurately perform visual inspection determine acceptability of product from visual defects and other overall cosmetic requirements.
Follow specific internal and customer specifications to determine product conformance.
Act as a trainer for other Inspector–I employees.
Complete inspection reports and product traveler as required.
Keep track of quantities and scrap codes and enter data into MRP system as applicable.
Provide feedback to supervisors and engineering on visual defects found.
Support visual inspection of validation activities as requested.
Qualifications
Experience using a microscope is required.
Communication skills verbal and written is required.
Experience in medical device manufacturing is preferred.
Must be able to work with minimal supervision and follow written instruction and schedules.
Must be detail oriented, focused and organized.
Must maintain work areas in a safe and orderly condition at all times.
Must comply with all applicable safety procedures.
Must be able to use microscope for extended periods of time.
Education Requirements
High School Diploma or equivalent is required.