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.