Quality Engineer Intern – Medical Devices (On‑Site)

Regulatory Jobs; Coon Rapids (MN); On-site; USD 28,000 - 40,000; Full time

Benefits offered by this job

Housing stipend for relocation

Health and wellness benefits

Career development activities

Opportunities to interact with leaders

Company events

Job summary

Cretex Medical is seeking a Quality Engineer Intern to provide technical support for quality projects and assist the Engineering department from scope through implementation. The role is located on-site in Coon Rapids, MN or Anoka, MN and requires 40 hours per week.

You will work with diverse teams to improve processes, read blueprints, use measuring devices, and ensure compliance with ISO and medical device requirements while developing hands-on experience in a fast-paced environment.

Qualifications

• Enrollment in a four-year degree program for Manufacturing, Mechanical, or Industrial Engineering.

Responsibilities

• Provide internal customer technical support.
• Part manufacturability technical support.
• Assist with the implementation of process and design improvements.
• Support and comply with the company Quality System, ISO, and medical device requirements.
• Read, understand, and follow work instructions and standard work.
• Partner with other business segments: sales/marketing, customer service, engineering, quality, and finance.
• Understand customer needs and the core business markets we serve.

Skills

Blueprint reading

Measuring devices

Interpersonal skills

Follow-through

Problem solving

MS Office proficiency

Verbal and written communication

Attention to detail

Teamwork

Multitasking

Education

Four-year degree program in Manufacturing/Mechanical/Industrial Engineering

Tools

Microsoft Office

Job description

Cretex Medical is seeking a Quality Engineer Intern to provide technical support for quality projects and assist the Engineering department from scope through implementation. The role is located on-site in Coon Rapids, MN or Anoka, MN and requires 40 hours per week.

You will work with diverse teams to improve processes, read blueprints, use measuring devices, and ensure compliance with ISO and medical device requirements while developing hands-on experience in a fast-paced environment.