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Internship Quality Engineer Medical Device Jobs (NOW HIRING)

IT MINDS L.L.C.

Quality Engineer - Medical Device

Newark, DE · On-site

$70K - $90K/yr

Quality Engineer - Medical Device Location: Delaware Largescale Medical Device client facing a remediation project here on site in Delaware. What is the project the contractor will be working on? • ...

Kellton Tech

Medical Device Quality Engineer

Madison, WI · On-site

$40 - $45/hr

Medical Device Quality Engineer Location: Madison, WI Pay Rate : $40--45/hr on W2 Schedule: Onsite, Monday-Friday (standard business hours) Summary The Senior Quality Analyst/Engineer is responsible ...

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How much do internship quality engineer medical device jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for internship quality engineer medical device in the United States is $36.72, according to ZipRecruiter salary data. Most workers in this role earn between $24.76 and $45.91 per hour, depending on experience, location, and employer.

What is the difference between Internship Quality Engineer Medical Device vs Quality Engineer Medical Device?

AspectInternship Quality Engineer Medical DeviceQuality Engineer Medical Device
QualificationsEnrolled in or recent graduate of relevant engineering or life sciences programBachelor's degree or higher in engineering, life sciences, or related field; certifications like CQE are common
Work EnvironmentInternship setting, supervised, entry-level tasksFull-time professional role, responsible for quality processes and compliance
ResponsibilitiesAssisting in quality audits, documentation, and process improvementLeading quality assurance activities, audits, and process optimization

The Internship Quality Engineer Medical Device role is an entry-level position designed for students or recent graduates gaining industry experience. In contrast, the Quality Engineer Medical Device is a full-time professional role with greater responsibilities in maintaining quality standards, compliance, and process improvements within the medical device industry.

What are the key skills and qualifications needed to thrive as an Internship Quality Engineer in Medical Devices, and why are they important?

To thrive as an Internship Quality Engineer in Medical Devices, you need a basic understanding of quality assurance principles, regulatory standards (such as ISO 13485 or FDA regulations), and coursework in biomedical, mechanical, or related engineering fields. Familiarity with quality management systems (QMS), data analysis tools, and document control software is typically required. Strong attention to detail, analytical thinking, and effective communication help interns excel in identifying and addressing quality issues. These skills are crucial for ensuring product safety, regulatory compliance, and maintaining high standards in the medical device industry.

What does an Internship Quality Engineer do in the medical device industry?

An Internship Quality Engineer in the medical device industry assists in ensuring that products meet regulatory standards and company quality requirements. Their responsibilities typically include participating in product testing, documenting results, supporting root cause analysis for defects, and helping to improve manufacturing processes. Interns may also assist in reviewing quality documentation, conducting audits, and working with cross-functional teams to maintain compliance with standards like ISO 13485 and FDA regulations. This role provides valuable hands-on experience in quality assurance and regulatory affairs within the medical device sector.

What types of projects and responsibilities can an Internship Quality Engineer expect in the medical device industry?

As an Internship Quality Engineer in the medical device field, you can expect to work on projects related to product inspections, documentation review, and process validation. You may assist in investigating non-conformances, supporting root cause analysis, and helping with risk assessments under the guidance of senior engineers. Interns often collaborate with cross-functional teams, including manufacturing, R&D, and regulatory affairs, to ensure products meet strict quality and compliance standards. This hands-on experience provides valuable insight into industry regulations and quality management systems, setting a strong foundation for future roles.
What cities are hiring for Internship Quality Engineer Medical Device jobs? Cities with the most Internship Quality Engineer Medical Device job openings:
What are the most commonly searched types of Quality Engineer Medical Device jobs? The most popular types of Quality Engineer Medical Device jobs are:
What states have the most Internship Quality Engineer Medical Device jobs? States with the most job openings for Internship Quality Engineer Medical Device jobs include:
Internship Quality Engineer Medical Device jobs near you
Quality Engineer Medical Device

Quality Engineer Medical Device

Egg Medical Inc

Roseville, MN • On-site

$100K - $115K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 21 days ago

Job description

Summary

We are seeking a Quality Engineer to add to our team! This position will support the management of our quality system while actively contributing to new product design and development initiatives. This role combines core quality engineering responsibilities with technical involvement in engineering projects to ensure our innovative medical devices meet the highest standards of safety, reliability, and regulatory compliance. 

Key Responsibilities

  • Quality System Support: Develop, implement, and maintain elements of the Quality Management System (QMS) to ensure ongoing compliance with FDA regulations, ISO 13485, and other applicable standards.
  • New Product Development & Design Control: Collaborate with R&D, engineering, and cross-functional teams on new design projects; support design inputs/outputs, risk assessments (e.g., FMEA, ISO 14971), design verification and validation activities, and design reviews/transfer to manufacturing.
  • Risk Management & Technical Reviews: Perform and document risk analyses, participate in technical design reviews, and ensure design controls are effectively applied throughout the product lifecycle.
  • Non-Conformance & Corrective Actions: Investigate non-conformances, lead root cause analysis, and implement corrective and preventive actions (CAPA) to drive continuous improvement and prevent recurrence.
  • Documentation & Compliance: Maintain accurate quality records, support internal/external audits, and contribute to regulatory submissions as needed.
  • Continuous Improvement: Identify opportunities to improve quality processes, product designs, and overall efficiency; partner with engineering and other teams on quality initiatives

Qualifications

  • Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Quality Engineering, or a related field.
  • 3+ years of experience as a Quality Engineer in a regulated industry, preferably medical devices.
  • Experience with FDA regulations, ISO 13485, and other medical device quality standards.
  • Proficiency in quality tools and methodologies (e.g., FMEA, SPC, CAPA).

Compensation & Benefits

  • Full-time position with salary range from $100,000-$115,000, depending on experience.
  • Additional bonus/incentive compensation available.
  • Company laptop provided.
  • Insurance available on the 1st of the month following date of hire, including: health, dental and vision insurance, plus pre-tax or Roth 401k available after 30 days.
  • PTO accrues starting at 15 days, plus 11 company paid holidays.

Company Description

Egg Medical is an innovative leader in radiation safety protection technology. Our mission is to protect healthcare professionals from occupational radiation exposure while enabling the delivery of exceptional patient care.