Precision QA Technician — Medical Devices Inspector

Zimmer Biomet; Lexington (KY); On-site; USD 52,000 - 76,000; Full time

Job summary

Zimmer Biomet in Lexington, KY, seeks a QA Inspector to perform dimensional inspections on machined and molded components, read engineering drawings, and maintain QA records. The role emphasizes accuracy, regulatory compliance, and cross-functional collaboration.

You will participate in first article and final inspections, specification verification, and documentation. Experience with ISO standards and medical device manufacturing is valued.

Qualifications

• Minimum 5 years of QA inspection experience.
• Experience with ISO and regulatory environments preferred.
• Strong documentation and record-keeping.
• Reading engineering drawings and specifications.

Responsibilities

• Perform dimensional inspections on machined and molded components from engineering drawings and standards.
• Perform first article and final product inspections using micrometers, calipers, optical comparator, and gages.
• Perform receiving inspection of Finished Goods and components.
• Perform component testing using tensile testers and force gauges.
• Complete QA paperwork and records including NCRs and QA history logs.
• Support qualification/validation of new products/processes.
• Follow procedures and update documents as needed.
• Interact with Manufacturing, Materials, and Engineering to improve product quality.
• Generate Non-conformance Reports and coordinate disposition of non-conforming products.
• Publish daily quality reports.
• Use MS Office for data entry and procedure updates.

Skills

Dimensional inspection

Measurement tools

Engineering drawings

Quality documentation

Regulatory knowledge

Attention to detail

Independent worker

Education

High school diploma or GED

Tools

Micrometers

Calipers

Optical comparator

Gages

Tensile testers

Job description

Zimmer Biomet in Lexington, KY, seeks a QA Inspector to perform dimensional inspections on machined and molded components, read engineering drawings, and maintain QA records. The role emphasizes accuracy, regulatory compliance, and cross-functional collaboration.

You will participate in first article and final inspections, specification verification, and documentation. Experience with ISO standards and medical device manufacturing is valued.