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Full Time Medical Device Product Development Jobs

Ventura Solutions LLC

Sales Engineer

Barrington, IL · On-site +1

Leverage knowledge of medical device product development processes to identify opportunities where ... Location * Lake Barrington, IL or Remote for the right candidate Employment Type * Full-time ...

Ventura Solutions LLC

Sales Engineer

Barrington, IL · On-site

Leverage knowledge of medical device product development processes to identify opportunities where ... Location * Lake Barrington, IL or Remote for the right candidate Employment Type * Full-time ...

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Full Time Medical Device Product Development information

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$127K

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

As of Aug 10, 2026, the average yearly pay for full time medical device product development in the United States is $126,987.00, according to ZipRecruiter salary data. Most workers in this role earn between $114,500.00 and $143,000.00 per year, depending on experience, location, and employer.
What cities are hiring for Full Time Medical Device Product Development jobs? Cities with the most Full Time Medical Device Product Development job openings:
What are the most commonly searched types of Medical Device Product Development jobs? The most popular types of Medical Device Product Development jobs are:
What states have the most Full Time Medical Device Product Development jobs? States with the most job openings for Full Time Medical Device Product Development jobs include:
Full Time Medical Device Product Development jobs near you

Medical Device Component Development Engineer

PB consulting

Loveland, OH

Full-time

Posted 3 days ago

New

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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