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Contract Medical Device Design Jobs in Ohio (NOW HIRING)

The ideal candidate will have expertise in design controls, verification & validation, supplier ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:

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Contract Medical Device Design information

What is the difference between Contract Medical Device Design vs Medical Device Design Engineer?

AspectContract Medical Device DesignMedical Device Design Engineer
CredentialsTypically requires a degree in engineering or related field; certifications like ISO 13485 are a plusRequires a degree in biomedical, mechanical, or electrical engineering; professional certifications may enhance prospects
Work EnvironmentProject-based, often freelance or consulting; varies by client and project scopeFull-time employment within a company or R&D department
Employer & Industry UsageUsed by consulting firms, contract agencies, and medical device startupsEmployed by medical device companies, hospitals, or research institutions

Contract Medical Device Design professionals focus on project-specific work, often freelance, while Medical Device Design Engineers are typically employed full-time within organizations. Both roles require similar technical credentials but differ in work setting and employment structure.

What are the most commonly searched types of Medical Device Design jobs in Ohio?

The most popular types of Medical Device Design jobs in Ohio are:

What cities in Ohio are hiring for Contract Medical Device Design jobs?

Cities in Ohio with the most Contract Medical Device Design job openings:

Medical Device Component Development Engineer

PB consulting

OH

Full-time

Posted 9 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