Quality Engineering Intern

Posted 2 Days Ago
Be an Early Applicant
Cartago, Cartago, CRI
In-Office
Internship
Healthtech
The Role
Support incoming inspection quality programs, monitor corrective actions, document QMS and GxP control activities, and help update supplier documentation to ensure compliance with medical device quality regulations.
Summary Generated by Built In

INTERNSHIP SCOPE

The Quality Engineering Intern will be supporting critical programs related to monitoring and follow up corrective actions for the incoming inspection area. The Intern will have high exposure to multidisciplinary teamwork and relationships. This role will develop and implement best practices focused on preventing defects, reducing variations, and driving continuous improvement to meet protocols.

EXPOSURE TO THE FOLLOWING RESPONSIBILITIES

  • Validate compliance with ISO 13485 y 21CFR 820 quality system regulations.
  • Analyze, review, and implement new processes that contribute to the improvement of the QMS.
  • Document SGC and GxP control activities with mentoring from other team members.
  • Draft and update supplier documentation through the change order process (CO-ASL) to proactively comply with applicable internal and external standards and regulations.


Requirements
  • Advanced university studies in engineering or life sciences.
  • Demonstrate interest in career development in medical devices.
  • Basic understanding of manufacturing, quality and engineering processes in a highly regulated industry, such as medical device, pharmaceutical, aerospace, automotive, etc.
  • Basic computer skills required (AutoCAD desirable)
  • Intermediate-advanced English level

Benefits

Interns will receive a subsidy package to support expenses such as transportantion, meals, equipment among others.

Skills Required

  • Advanced university studies in engineering or life sciences
  • Demonstrated interest in a career in medical devices
  • Basic understanding of manufacturing, quality, and engineering processes in regulated industries
  • Basic computer skills
  • AutoCAD
  • Intermediate-advanced English level
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The Company
HQ: Saint Paul, MN
172 Employees
Year Founded: 2000

What We Do

Nextern collaborates with innovators, clinicians, and device partners to create, iterate, optimize and manufacture best-in-class medical devices. We bring an unmatched core competence in medical device product design and development through manufacturing as a leverageable asset to collaborators like you, who are focused on accelerating the commercial side of the business.​

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