Entry to mid-level quality inspection role in a high-end medical device environment. Responsible for final inspections, ensuring all parts meet shipment-ready quality standards before delivery.

Responsibilities: 

Perform final inspections on completed parts. Verify parts meet specifications and quality standards. Identify defects and surface imperfections. Document inspection results. Support corrective actions when nonconformances are identified. Work in compliance with ISO 9001 and ISO 13485 standards.

Qualifications: 

1–2 years manufacturing inspection experience. Comfortable working in ISO 9001 or ISO 13485 environment. Strong attention to small defects and surface quality. Basic blueprint reading capability. Reliable and detail-oriented. High School Diploma or GED.

Work Environment: Precision, climate-controlled medical device facility. Regulated and quality-driven environment. Day shift focus. Uniforms and sa...