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Medical Device Engineer Part Time Jobs (NOW HIRING)

IQVIA

MedTech Medical Device Clinical Trial

Boston, MA

$50 - $60/hr

Gain professional growth and exposure to the medical device industry You will have an opportunity ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

Hanger, Inc.

HFN: QA/QC Engineer II

Phoenix, AZ · On-site

$71.50K - $92.30K/yr

Experience in manufacturing of medical device with electronic components is preferred. * Broad ... Flexible Work Schedules and Part-time Opportunities * Generous Employee Referral Bonus Program

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How much do medical device engineer part time jobs pay per hour?

As of May 30, 2026, the average hourly pay for medical device engineer part time in the United States is $49.84, according to ZipRecruiter salary data. Most workers in this role earn between $35.10 and $59.62 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Medical Device Engineer Part Time, and why are they important?

To thrive as a Medical Device Engineer Part Time, you need a background in biomedical engineering or a related field, knowledge of medical device regulations, and strong problem-solving skills. Familiarity with CAD software, prototyping tools, and regulatory standards like FDA or ISO 13485 is typically required. Strong communication, attention to detail, and teamwork abilities help you effectively collaborate and ensure device safety. These skills are crucial for developing compliant, innovative medical devices that meet rigorous industry standards while working efficiently in a part-time capacity.

What are some common challenges faced by part-time Medical Device Engineers, and how can they effectively manage project responsibilities?

Part-time Medical Device Engineers often face challenges such as balancing project deadlines with limited working hours and ensuring seamless communication with full-time team members. Effective time management and proactive coordination are key to overcoming these obstacles. Utilizing collaborative tools, regularly updating progress, and clarifying expectations with supervisors can help part-time engineers stay aligned with project goals and maintain productivity within their flexible schedules.

What does a Medical Device Engineer Part Time do?

A Medical Device Engineer Part Time designs, develops, tests, and improves medical devices on a reduced or flexible work schedule. Their responsibilities may include assisting with product design, ensuring regulatory compliance, troubleshooting device issues, and collaborating with cross-functional teams. Part-time engineers often focus on specific tasks or projects, providing their expertise without committing to a full-time schedule. This role is ideal for those seeking work-life balance or looking to contribute specialized skills to medical device innovations.

What is the difference between Medical Device Engineer Part Time vs Medical Device Technician Part Time?

AspectMedical Device Engineer Part TimeMedical Device Technician Part Time
Required CredentialsBachelor's degree in engineering or related field; certifications varyTechnical diploma or associate degree; certifications may be required
Work EnvironmentDesign labs, R&D departments, manufacturing facilitiesMaintenance, testing, and repair in clinical or manufacturing settings
Employer & Industry UsageMedical device companies, biotech firms, hospitalsHospitals, clinics, medical device manufacturing
Common Search & ComparisonMedical Device Engineer Part Time vs Medical Device Technician Part Time

Medical Device Engineer Part Time roles focus on designing, developing, and improving medical devices, requiring engineering skills and often a degree in engineering. In contrast, Medical Device Technician Part Time positions involve maintaining, testing, and repairing devices, typically requiring technical training. Both roles are essential in the medical device industry but differ in responsibilities, work environment, and required credentials.

What cities are hiring for Medical Device Engineer Part Time jobs? Cities with the most Medical Device Engineer Part Time job openings:
What are the most commonly searched types of Medical Device Engineer jobs? The most popular types of Medical Device Engineer jobs are:
What states have the most Medical Device Engineer Part Time jobs? States with the most job openings for Medical Device Engineer Part Time jobs include:
Medical Device Engineer Part Time jobs near you

Remote | Medical Device Quality & Regulatory Workflow Specialist -- $60-$85/hour

24-MAG

New York, NY • Remote

$60 - $85/hr

Part-time

Posted 4 days ago

Job description

We are sharing a specialised part-time consulting opportunity for professionals experienced in medical devices, regulatory affairs, quality engineering, design controls, manufacturing validation, supplier quality, clinical affairs, and structured regulated-device documentation.

This role supports current and upcoming remote consulting opportunities focused on structured medical device workflow review, regulatory documentation, quality system assessment, design history file review, validation documentation, CAPA analysis, and high-quality project execution. Selected professionals will apply their medical device expertise to review realistic regulated-device scenarios, evaluate technical and compliance requirements, prepare structured written outputs, and support accurate, evidence-based medical device workflow tasks.

Key Responsibilities

Professionals in this role may contribute to:

Regulatory Affairs & Submission Documentation

  • Review medical device scenarios involving 510(k), PMA, De Novo, EU MDR, technical files, regulatory submissions, and supporting documentation
  • Evaluate regulatory materials against source records, device requirements, submission expectations, and documented review criteria
  • Support structured review of regulatory correspondence, submission packages, technical documentation, and device classification materials
  • Identify missing information, documentation gaps, regulatory inconsistencies, and expected submission review outcomes

Quality Systems, Risk & CAPA Review

  • Review quality scenarios involving DHF, DMR, risk-analysis matrices, CAPA records, eQMS workflows, validation protocols, and quality documentation
  • Evaluate materials against 21 CFR 820, ISO 13485, ISO 14971, design control requirements, risk management expectations, and quality system procedures
  • Support structured review of CAPA documentation, risk files, quality records, post-market surveillance materials, and MDR/vigilance reporting workflows
  • Prepare clear written explanations for quality and regulatory decisions based on source materials and verifiable criteria

Design Controls, Manufacturing & Validation Support

  • Review device R&D and manufacturing scenarios involving design controls, software-related device workflows, process validation, supplier quality, and manufacturing engineering documentation
  • Evaluate validation protocols, supplier records, manufacturing workflows, and device development materials against defined technical requirements
  • Support structured review of materials connected to ANSYS Fluent, STAR-CCM+, Siemens Opcenter, Rockwell FactoryTalk, DocuSign, eQMS systems, or similar regulated-device tools
  • Maintain accuracy, consistency, and professional judgment across submitted work

Ideal Profile

Strong candidates may have:

  • 3+ years of experience in medical devices, regulatory affairs, quality engineering, design controls, R&D, manufacturing engineering, process validation, supplier quality, clinical affairs, post-market surveillance, or related regulated-device roles
  • Experience in one or more areas such as 510(k), PMA, De Novo, EU MDR, technical files, 21 CFR 820, ISO 13485, ISO 14971, CAPA, DHF, DMR, SaMD, process validation, supplier quality, or vigilance reporting
  • Familiarity with tools and systems such as ANSYS Fluent, STAR-CCM+, Siemens Opcenter, Rockwell FactoryTalk, DocuSign, eQMS platforms, PLM systems, MES platforms, or similar medical device workflow tools
  • Comfort reading and preparing medical device artifacts such as design history files, regulatory submissions, DHF/DMR documents, risk-analysis matrices, validation protocols, CAPA records, supplier files, and technical summaries
  • Strong analytical thinking and written communication skills
  • Ability to translate regulated medical device workflows into clear, structured task documentation

Educational Background

  • A degree or professional background in biomedical engineering, mechanical engineering, electrical engineering, regulatory affairs, quality engineering, life sciences, clinical research, manufacturing engineering, or a related field is helpful
  • Equivalent practical experience in medical device regulatory, quality, R&D, manufacturing, clinical affairs, or validation workflows is also highly relevant

Nice to Have

  • Experience at a medical device manufacturer, contract developer, contract manufacturer, healthcare technology company, or regulated life sciences organization
  • Familiarity with design controls, risk management, FDA submissions, EU MDR, SaMD, eQMS, supplier quality, process validation, CAPA, clinical affairs, or post-market surveillance
  • Experience preparing or reviewing regulatory submissions, technical files, validation protocols, DHF/DMR materials, CAPA records, risk files, or quality documentation
  • RAC, ASQ CQE, CRE, CBA, regulatory affairs, quality, validation, or medical device certifications are helpful
  • Strong attention to detail in regulated, documentation-heavy, and cross-functional medical device environments

Why This Opportunity

  • Apply medical device regulatory, quality, and engineering expertise to structured remote project work
  • Contribute to high-quality device documentation review, regulatory workflow assessment, quality system analysis, and validation scenario development
  • Work on flexible, project-based assignments aligned with your medical device background
  • Use your regulated-device judgment in a focused, detail-oriented review environment
  • Remote structure with competitive hourly compensation

Contract Details

  • Independent contractor role
  • Fully remote with flexible scheduling
  • Part-time commitment depending on project availability
  • Competitive rates between $60–$85 per hour depending on expertise
  • Weekly payments via Stripe or Wise
  • Projects may be extended, shortened, or adjusted depending on scope and performance
  • Work will not involve access to confidential or proprietary information from any employer, client, or institution

About the Platform

This opportunity is available through 24-MAG LLC. We connect experienced professionals with remote consulting opportunities across technical, evaluation, and project-based workstreams.

By submitting this application, you acknowledge that your information may be processed by 24-MAG LLC for recruitment and opportunity matching in accordance with our Privacy Policy: https://www.24-mag.com/privacy-policy.