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Junior Medical Device Product Development 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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Junior Medical Device Product Development information

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$33.5K

$71.8K

$109.5K

How much do junior medical device product development jobs pay per year?

As of Aug 17, 2026, the average yearly pay for junior medical device product development in the United States is $71,799.00, according to ZipRecruiter salary data. Most workers in this role earn between $48,500.00 and $80,000.00 per year, depending on experience, location, and employer.

What is a junior medical device product development professional?

A Junior Medical Device Product Development professional assists in designing, developing, and testing new medical devices under the supervision of more experienced engineers and project managers. Their responsibilities often include research, prototyping, documentation, and ensuring products meet regulatory requirements. They collaborate with cross-functional teams such as engineering, marketing, and quality assurance to bring safe and effective medical devices to market. This entry-level role is ideal for recent graduates or those with limited experience who are interested in the medical technology field.

What are the key skills and qualifications needed to thrive as a junior medical device product development professional?

To thrive as a Junior Medical Device Product Development professional, you need a solid background in biomedical engineering or a related field, with knowledge of regulatory standards and product lifecycle management. Familiarity with CAD software, prototyping tools, and quality management systems is typically required, and certifications like ISO 13485 can be advantageous. Strong problem-solving abilities, attention to detail, and effective teamwork and communication skills help you excel in collaborative, multidisciplinary environments. These competencies are crucial to ensure the safe, compliant, and innovative development of medical devices that meet both user needs and regulatory requirements.

What are some common challenges faced by junior professionals in medical device product development and how can they overcome them?

Junior professionals in medical device product development often encounter challenges such as navigating complex regulatory requirements, understanding interdisciplinary collaboration, and rapidly adapting to evolving technologies. To overcome these, it's essential to actively seek mentorship from experienced team members, participate in cross-functional meetings, and stay updated with industry standards and regulations. Developing strong communication skills and a willingness to learn from feedback can also help juniors contribute effectively and grow within the team.

What is the difference between Junior Medical Device Product Development vs Medical Device Quality Assurance Specialist?

AspectJunior Medical Device Product DevelopmentMedical Device Quality Assurance Specialist
CredentialsTypically requires a degree in engineering, biomedical, or related field; certifications like ISO 13485 are a plusRequires a degree in life sciences, engineering, or related; certifications such as CQE or ISO 13485 auditor are common
Work EnvironmentDesign labs, R&D departments, cross-functional teamsQuality labs, compliance departments, manufacturing settings
Employer & Industry UsageMedical device companies, startups, R&D divisionsManufacturers, regulatory agencies, compliance firms

Junior Medical Device Product Development focuses on designing and developing new medical devices, while Medical Device Quality Assurance Specialists ensure products meet quality standards and regulatory requirements. Both roles are essential in the medical device industry but serve different functions within the product lifecycle.

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Junior Medical Device Product Development jobs near you
Infographic showing various Junior Medical Device Product Development job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $71,799 per year, or $34.5 per hour.

Medical Device Component Development Engineer

PB consulting

Kenwood, OH • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

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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