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Internship Quality Engineer Medical Device Jobs (NOW HIRING)

Synkriom

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Medical Device Quality Engineer

Warsaw, IN · On-site

$35 - $40/hr

Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preferred Company Description Founded in 2015 and backed by two decades of hands-on experience, our ...

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 ...

CSL Plasma Inc.

$115 - $136/hr

... quality engineering techniques such as risk analysis, statistical data analysis, sampling plan development, etc. * Ensure external medical device development and manufacturing partners meet the ...

Caraballo Consulting & Associates L

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QA Manufacturing Engineer - Medical Device

Sterling, VA · On-site

$40 - $80/hr

We are seeking a Quality Manufacturing Engineer extensive experience in Medical Devices to oversee Manufacturing Quality projects and line transfers for a Medical Device company. The perfect ...

Caraballo Consulting & Associates L

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QA Manufacturing Engineer - Medical Device

Sterling, VA · On-site

$40 - $80/hr

We are seeking a Quality Manufacturing Engineer extensive experience in Medical Devices to oversee Manufacturing Quality projects and line transfers for a Medical Device company. The perfect ...

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

As of Sep 6, 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 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 are the key skills and qualifications needed to thrive as an internship quality engineer in medical devices?

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 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 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 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

Medical Device Design Quality Engineer

Experis

Pittsburgh, PA • On-site

$37 - $42/hr

Other

Medical, Dental, Vision, Life, Retirement

Posted 9 days ago

Job description

Our client, a leading organization in the medical device industry, is seeking a Medical Device Design Quality Engineer to join their team. As a Medical Device Design Quality Engineer, you will be part of the Quality Assurance department supporting product development and manufacturing teams. The ideal candidate will demonstrate strong analytical skills, attention to detail, and a proactive mindset, which will align successfully in the organization.

Job Title: Medical Device Design Quality Engineer

Location: Pittsburgh, PA (Onsite)

Pay Range: $37-$42/Hr. on W2

What's the Job?

  • Support design quality activities throughout new product development, including design reviews, requirements review, risk management, verification and validation planning, and design transfer readiness.
  • Lead and participate in Design Failure Modes and Effects Analysis (DFMEA) and risk assessments to identify and mitigate design and manufacturing risks.
  • Review protocols and participate in V&V planning to ensure alignment with product requirements and risk controls.
  • Support design transfer activities by ensuring product and process requirements are translated into manufacturing, inspection, supplier, validation, and release deliverables.
  • Manage and drive timely resolution of nonconformances (NCs) and corrective & preventive actions (CAPAs).

What's Needed?

  • Bachelor's degree in Engineering, Quality, or a related field (Master's preferred).
  • 3+ years of experience in medical device quality engineering or a related field.
  • Strong knowledge of ISO 13485, FDA QSR (21 CFR Part 820), EU MDR, and risk management (ISO 14971).
  • Experience with Design Control, Process Validation, CAPA, and Supplier Quality.
  • Proficiency in statistical analysis tools (Minitab) and problem-solving methodologies (8D, DMAIC).

What's in it for me?

  • Opportunity to work in a dynamic and innovative environment.
  • Immediate start with potential for long-term career growth.
  • Collaborate with a dedicated team of professionals in the medical device industry.
  • Engage in meaningful work that impacts patient safety and healthcare advancements.
  • Supportive work culture emphasizing continuous improvement and professional development.

Upon completion of waiting period consultants are eligible for:

  • Medical and Prescription Drug Plans
  • Dental Plan
  • Vision Plan
  • Health Savings Account
  • Health Flexible Spending Account
  • Dependent Care Flexible Spending Account
  • Supplemental Life Insurance
  • Short Term and Long Term Disability Insurance
  • Business Travel Insurance
  • 401(k), Plus Match
  • Weekly Pay

If this is a role that interests you and you'd like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!

About ManpowerGroup, Parent Company of: Manpower, Experis and Talent Solutions.

Experis® is a global leader in technology services and part of the ManpowerGroup® (NYSE: MAN) family of brands. We connect skilled technology professionals with meaningful opportunities where they can grow their careers, expand their expertise and make a real impact. Guided by the belief that it takes Human Ingenuity to unlock the true potential of technology, Experis helps people gain experience with leading organizations, build sought-after skills and take the next step toward a brighter future. Backed by ManpowerGroup's 75+ years of workforce expertise and global reach across more than 70 countries and territories, Experis brings the scale, insight and opportunity to help people and businesses thrive. ManpowerGroup is consistently recognized for its commitment to inclusion, ethics and responsible business, including being named one of the World's Most Ethical Companies. Learn more at Experis.com.

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