Quality Inspector I — Medical Devices & Growth

Cirtec Services GmbH; Sturtevant (WI); On-site; USD 26,000 - 34,000; Full time

Job summary

Cirtec Medical Corporation in Wisconsin is seeking a Quality Control Inspector to perform receiving, in-process, and final inspections of medical device components. You will document results, maintain traceability, and communicate status to engineering and production teams.

The role requires reading blueprints, using microscopes and measuring tools, and ensuring compliance with ISO 13485 and FDA QSR. Prior QA experience in medical manufacturing is preferred.

Qualifications

• High school diploma or GED required; certs in medical/QA preferred.
• Proven experience inspecting and documenting results in a regulated industry.
• Able to read technical drawings, blueprints, and GD&T.
• Fluent in reading/writing/speaking English; proficient with PCs and MS Office.

Responsibilities

• Inspect or test incoming parts, assemblies, and finished products for conformance to specifications; record results.
• Maintain product identification and traceability; indicate status with labels and stamps.
• Control non-conforming products per procedures; initiate non-conformance reports when needed.
• Assist with process documentation control and equipment calibration.
• Participate in internal audits; support quality records and documentation updates.
• Communicate status of products to supervisors and engineering teams as required.

Skills

Quality Inspection

Microscope operation

Reading blueprints & drawings

English fluency

Quality documentation

Education

High school diploma or GED

Certificate in medical quality assurance

Tools

Measuring equipment

PC/MS Office

Job description

Cirtec Medical Corporation in Wisconsin is seeking a Quality Control Inspector to perform receiving, in-process, and final inspections of medical device components. You will document results, maintain traceability, and communicate status to engineering and production teams.

The role requires reading blueprints, using microscopes and measuring tools, and ensuring compliance with ISO 13485 and FDA QSR. Prior QA experience in medical manufacturing is preferred.