Onsite Quality Inspector — Medical Devices (Jackson, MI)

Envista Holdings Corporation; Jackson (MI); On-site; USD 30,307 - 37,195; Full time

Job summary

Envista Holdings Corporation in Jackson, Michigan, is seeking a Quality Inspector to perform incoming, in-process, and final inspections of medical device components and finished goods onsite. You will verify conformance to drawings and standards using precision tools and document results according to the QMS.

The role requires reading engineering drawings, knowledge of GMP and ISO 13485 after training, and the ability to work independently within a cross-functional team.

Qualifications

• High school minimum.
• Ability to read and interpret engineering drawings and technical specifications.
• Knowledge of FDA Quality System requirements (GMP) and ISO 13485 after training.
• Familiarity with inspection tools and measurement techniques.
• Oral communication – speaks clearly and persuasively; listens and seeks clarification.
• Ability to work independently and in a cross-functional team environment.

Responsibilities

• Perform incoming, in-process, and final inspections of medical device components and finished goods.
• Verify conformance against drawings, specifications, and quality standards.
• Utilize calipers, micrometers, gauges, and visual devices to assess dimensions.
• Document inspection results and maintain records in the QMS.
• Identify, document, and report nonconformances.
• Assist in developing and improving inspection procedures and quality processes.

Skills

Oral communication

Independent worker

Cross-functional teamwork

Quality inspection

Education

High school diploma or equivalent

Tools

Calipers

Micrometers

Gauges

Visual measuring devices

Job description

Envista Holdings Corporation in Jackson, Michigan, is seeking a Quality Inspector to perform incoming, in-process, and final inspections of medical device components and finished goods onsite. You will verify conformance to drawings and standards using precision tools and document results according to the QMS.

The role requires reading engineering drawings, knowledge of GMP and ISO 13485 after training, and the ability to work independently within a cross-functional team.