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

As of Aug 8, 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?

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

Senior Medical Device Quality Engineer

Prophecy Technologies

Blue Ash, OH • On-site

$81K - $110K/yr

Full-time

Posted 9 days ago

Job description

Role Overview:
This Senior Medical Device Quality Engineer role involves leading multiple high-priority lifecycle change projects from concept through implementation within the medical device or other regulated industries. The position requires strong expertise in design controls, risk management, quality management systems, and process validation to ensure regulatory compliance and product quality.
Key Responsibilities:
  • Lead multiple high-priority lifecycle change projects from concept through implementation.
  • Drive project plans, timelines, risk mitigation strategies, and implementation readiness.
  • Coordinate cross-functional teams across Engineering, Quality, Regulatory, Manufacturing, Supply Chain, Procurement, Operations, and external suppliers.
  • Serve as the technical interface with suppliers for component development, DFM reviews, tooling readiness, process capability, and component qualification.
  • Support design verification and validation activities, including test planning, execution, data review, and technical documentation.
  • Partner with manufacturing sites on process validation activities, including IQ/OQ/PQ, pilot builds, validation builds, and production launch readiness.
  • Apply strong knowledge of design controls, engineering change management, risk management, quality system requirements, and regulatory expectations.
  • Review engineering drawings, specifications, GD&T requirements, tolerance analyses, and component acceptance criteria.
  • Drive root cause analysis, technical problem solving, and timely closure of project issues.
  • Communicate project status, risks, decisions, and recommendations clearly to stakeholders and senior leadership.
  • Demonstrate strong ownership, urgency, accountability, and ability to influence without direct authority.

Required Skills:
  • Strong expertise in Medical Device Product Lifecycle Management (PLM), Design Controls, and Engineering Change Management (ECO/ECN/ECR).
  • Hands-on experience with Design Verification & Validation (V&V), test methods, protocol development, and technical documentation.
  • Deep understanding of Risk Management methodologies, including ISO 14971, DFMEA, PFMEA, and hazard analysis.
  • Knowledge of Quality Management Systems (QMS), ISO 13485, FDA 21 CFR Part 820/QMSR, and regulatory compliance requirements.
  • Experience in Supplier Quality Engineering, component qualification, supplier development, and Design for Manufacturability (DFM).
  • Proficiency in Process Validation activities including IQ/OQ/PQ, pilot builds, validation builds, and manufacturing transfer.
  • Ability to interpret engineering drawings, GD&T, tolerance stack-ups, specifications, and acceptance criteria.
  • Strong root cause analysis and problem-solving skills utilizing 8D, CAPA, 5 Why, Fishbone, and corrective action processes.
  • Excellent project management skills, including planning, scheduling, risk management, stakeholder management, and cross-functional coordination.
  • Effective leadership, communication, and influencing skills.
  • EIS : MDD Risk Management.

Qualifications:
  • 6-8 years of experience required.
  • 7+ years of engineering experience in medical device or other regulated industries.
  • Experience leading cross-functional technical projects.
  • Experience with component development, supplier qualification, design verification, and manufacturing validation.
  • Strong understanding of design controls, change management, risk management, process validation, and quality system compliance.

Preferred Skills:
  • EIS : New Product Development (NPD) Methodology and Management.

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