Medical Device Quality Inspector – 2nd Shift

Cretex Medical Component and Device Technologies; Minneapolis (MN); On-site; USD 25,000 - 39,000; Full time

Job summary

Cretex Medical is seeking a Quality Inspector to perform first piece, in-process and final inspections on components and assemblies. You will review release documentation, inspect injections and assemblies, and ensure materials meet quality and dimensional standards.

Responsibilities include reading quality plans and specs, using metrology tools like CMM/OGP, and recording data with attention to detail while maintaining a clean 5S workspace and complying with GMP/ISO requirements.

Qualifications

• High school diploma or GED and basic measurement knowledge.
• Experience with inspection equipment, drawings, and quality records.
• Familiarity with GMP/ISO quality systems and documentation.

Responsibilities

• Perform first piece, in-process, and final inspections per quality plans.
• Review and approve final release documentation and incoming materials.
• Inspect injections, assemblies, and materials for quality, appearance, and performance.
• Read quality plans, blueprints and specifications; determine defects.
• Record hours worked and maintain 5S organized work area.
• Communicate inspection results with team; adhere to safety policies.

Skills

Inspection equipment use

Reading blueprints

Documentation

Communication skills

Microsoft Office

Mechanical aptitude

Attention to detail

Prioritize multiple tasks

Education

High School Diploma or GED

Tools

Tool Scope

CMM

OGP

Vision Systems

Metrology tools

Job description

Cretex Medical is seeking a Quality Inspector to perform first piece, in-process and final inspections on components and assemblies. You will review release documentation, inspect injections and assemblies, and ensure materials meet quality and dimensional standards.

Responsibilities include reading quality plans and specs, using metrology tools like CMM/OGP, and recording data with attention to detail while maintaining a clean 5S workspace and complying with GMP/ISO requirements.