Quality Engineer Intern: Hands-on QA & Process Impact

Medline Industries, LP

Northfield (MN)

On-site

USD 32,000 - 46,000

Full time

6 days ago
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Benefits offered by this job

401(k) contributions
Paid time off
Employee Assistance Program
Employee Resource Groups
Employee Service Corp for interns and:
Employee Service Corp for interns and:

Job summary

Medline offers a 10-week summer internship across its corporate offices, including social events, leadership presentations, and community activities. The Quality Engineer Intern will manage projects related to product quality, CAPA, risk analysis, and documentation for the Master Device Record.

Open to rising seniors in engineering or science programs, with a minimum 3.0 GPA. You’ll gain hands-on experience, design test plans, assist with FDA submissions, and develop strong documentation and

Qualifications

  • Engineering or Science related majors preferred.
  • Junior standing with 3.0 minimum GPA preferred.
  • Detail oriented with superior organizational, analytical, and problem-solving skills.
  • Motivated self-starter.
  • Good documentation skills and an attention to detail.
  • Design project experience.
  • Unrestricted permanent US work authorization.

Responsibilities

  • The Quality Engineer Intern position will entail managing multiple projects related to product quality (Design Files, Risk Analysis, CAPA process, 510k data collection, product testing).
  • Creating documentation for the Master Device Record and related quality files.
  • Supporting CAPAs, SCARs, supplier maintenance, risk analysis, and more.

Skills

Detail oriented with analytical and?

Education

Engineering or Science related majors
Junior standing with 3.0 minimum GPA

Job description

Medline offers a 10-week summer internship across its corporate offices, including social events, leadership presentations, and community activities. The Quality Engineer Intern will manage projects related to product quality, CAPA, risk analysis, and documentation for the Master Device Record.

Open to rising seniors in engineering or science programs, with a minimum 3.0 GPA. You’ll gain hands-on experience, design test plans, assist with FDA submissions, and develop strong documentation and

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