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Internship Medical Device Consulting Jobs (NOW HIRING)

PB consulting

We are seeking a Medical Device Component Development Engineer to support component development, product lifecycle management, and engineering change activities for regulated medical devices. The ...

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How much do internship medical device consulting jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for internship medical device consulting in the United States is $19.31, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $20.91 per hour, depending on experience, location, and employer.

What is an internship in medical device consulting?

An internship in medical device consulting is a temporary position where students or recent graduates gain hands-on experience working with consulting firms that specialize in advising medical device companies. Interns typically assist with projects related to regulatory compliance, product development, market analysis, and quality assurance. This role provides valuable exposure to the healthcare industry, helps interns develop problem-solving and communication skills, and can be a stepping stone to a career in medical device consulting or related fields.

What types of projects and responsibilities can I expect during an internship in medical device consulting?

As an intern in medical device consulting, you can expect to be involved in a range of projects, such as assisting with regulatory submissions, conducting market research, preparing technical documentation, and supporting client meetings. Many interns also help analyze data related to product safety, efficacy, and compliance with industry standards. You will likely work closely with experienced consultants, engineers, and regulatory specialists, gaining hands-on experience with real-world challenges faced by medical device companies. This collaborative environment offers valuable exposure to the consulting process and a chance to develop both technical and soft skills relevant to the medical device industry.

What are the key skills and qualifications needed to thrive as an internship medical device consulting?

To thrive as an intern in medical device consulting, you need a solid background in biomedical engineering, life sciences, or a related field, often supported by current enrollment in an undergraduate or graduate program. Familiarity with regulatory guidelines (such as FDA or ISO), data analysis tools, and project management software is highly beneficial. Strong analytical thinking, effective communication, and a collaborative mindset are standout soft skills in this role. These abilities ensure interns can contribute meaningfully to client projects, navigate complex compliance requirements, and support innovation within multidisciplinary teams.

What cities are hiring for Internship Medical Device Consulting jobs?

Cities with the most Internship Medical Device Consulting job openings:

What are the most commonly searched types of Medical Device Consulting jobs?

The most popular types of Medical Device Consulting jobs are:

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Internship Medical Device Consulting jobs near you

Medical Device Component Development Engineer

PB consulting

Terrace Park, OH • On-site

Full-time

Posted 6 days ago

Job description

We are seeking a Medical Device Component Development Engineer to support component development, product lifecycle management, and engineering change activities for regulated medical devices. The ideal candidate will have expertise in design controls, verification & validation, supplier quality, process validation, and regulatory compliance.

Roles and Responsibilities
  • Lead component development and engineering change projects from concept to implementation.
  • Manage project timelines, risks, and cross-functional coordination.
  • Support Design Verification & Validation (V&V), test protocols, and technical documentation.
  • Partner with suppliers on component qualification, DFM reviews, tooling, and process capability.
  • Support manufacturing transfer, IQ/OQ/PQ, pilot builds, and production readiness.
  • Apply Design Controls, PLM, ECO/ECN/ECR, Risk Management, and Quality System requirements.
  • Review engineering drawings, GD&T, specifications, and acceptance criteria.
  • Drive root cause analysis using CAPA, 8D, 5 Whys, and Fishbone methodologies.
  • Communicate project status, risks, and technical recommendations to stakeholders.
Required Qualifications
  • Experience in Medical Device Component Development or Product Development.
  • Strong knowledge of:
    • Product Lifecycle Management (PLM)
    • Design Controls & Engineering Change Management (ECO/ECN/ECR)
    • Design Verification & Validation (V&V)
    • ISO 14971, DFMEA, PFMEA
    • ISO 13485 & FDA 21 CFR Part 820/QMSR
    • Supplier Quality Engineering & Design for Manufacturability (DFM)
    • Process Validation (IQ/OQ/PQ)
    • GD&T and engineering drawings
  • Strong project management, communication, and problem-solving skills.
  • Experience working with cross-functional teams in a regulated medical device environment.
Preferred Skills
  • Medical Device Product Development
  • Supplier Quality & Component Qualification
  • Risk Management & Regulatory Compliance
  • Manufacturing Transfer & Validation
  • Root Cause Analysis (CAPA, 8D)
  • Stakeholder & Project Management

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