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Remote R&D Engineer Medical Device Jobs in Rutherford, NJ

Clinical Search Group, LLC

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Sales Territory Manager/Physician Liaison

Jamaica, NY · Remote

$90K - $120K/yr

Company Description Clinical Search Group, LLC is a full service Medical Device Recruiting Company specializing in finding and placing Clinicians, Field Clinical Engineers, Medical Science Liaisons ...

Tempus

Senior Quality Engineer

New York, NY · On-site +1

Be involved in the medical device software design controls activities, in accordance with the FDA ... Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote ...

Provident Research Inc

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Senior Clinical Research Associate Cardiac Medical Device

New York, NY · Remote

$135K - $141K/yr

SR CRA Cardiac Medical Device (home based) Remote Become Part of a Major Initiative to Monitor Life Saving Cardiovascular Devices This position will be working with a Provident Research Inc. in a ...

Torq

DevOps Engineer (Remote)

New York, NY · On-site +1

$57.75 - $79/hr

... Engineer to join our fast-growing company at a breakthrough stage - building our dream team with ... Build intuitive internal tools and foster a culture of self-service within R&D. * Lead deployments ...

Tempus

Lead Quality Engineer

New York, NY · On-site +1

$120K - $165K/yr

Apply medical device quality system knowledge as part of quality leadership, including but not ... Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote ...

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All JobsRemote R&D Engineer Medical Device JobsRemote R&D Engineer Medical Device Jobs in Rutherford, NJ

Remote R D Engineer Medical Device information

See Rutherford, NJ salary details

$37.7K

$108.1K

$145.3K

How much do remote r&d engineer medical device jobs pay per year?

As of Jun 9, 2026, the average yearly pay for remote r&d engineer medical device in Rutherford, NJ is $108,072.00, according to ZipRecruiter salary data. Most workers in this role earn between $106,000.00 and $106,000.00 per year, depending on experience, location, and employer.

What is the difference between Remote R&D Engineer Medical Device vs Remote Biomedical Engineer?

AspectRemote R&D Engineer Medical DeviceRemote Biomedical Engineer
Required CredentialsBachelor's or Master's in Engineering, Biomedical, or related fields; certifications varyBachelor's or Master's in Biomedical Engineering or related fields; certifications may include regulatory or clinical
Work EnvironmentPrimarily remote, collaborating with R&D teams, design, testing, and product developmentRemote or on-site, focusing on clinical applications, device integration, and research
Employer & Industry UsageMedical device companies, R&D labs, startupsHospitals, research institutions, medical device firms

The Remote R&D Engineer Medical Device and Remote Biomedical Engineer roles share similar educational backgrounds and often work in remote settings. However, the R&D engineer focuses more on product development and engineering design, while the biomedical engineer emphasizes clinical applications and research. Both roles are vital in advancing medical technology but differ in their primary focus and work environment.

What is a Remote R&D Engineer in the medical device industry?

A Remote R&D Engineer in the medical device industry is a professional who works from a location outside the traditional office or laboratory environment, focusing on the research and development of new medical devices or the improvement of existing ones. Their responsibilities typically include designing prototypes, conducting experiments, analyzing test data, and collaborating with cross-functional teams to ensure regulatory compliance and product safety. By working remotely, these engineers utilize digital tools to communicate and manage projects, allowing for flexibility while maintaining high standards of innovation and quality in medical device development.

How do Remote R&D Engineers for medical devices typically collaborate with cross-functional teams despite working offsite?

Remote R&D Engineers in the medical device industry often collaborate closely with colleagues in engineering, regulatory, quality, and clinical affairs through digital platforms. Regular video conferences, project management tools, and shared documentation systems ensure alignment across time zones and departments. Clear communication, detailed documentation, and proactive updates are essential for maintaining project momentum and meeting strict regulatory standards. While remote collaboration can be challenging initially, most organizations provide robust onboarding and support to help engineers integrate effectively with distributed teams.

What are the key skills and qualifications needed to thrive as a Remote R&D Engineer in Medical Devices, and why are they important?

To thrive as a Remote R&D Engineer in Medical Devices, you need a solid background in biomedical or mechanical engineering, product development experience, and a relevant degree such as a BS or MS. Familiarity with CAD software, regulatory standards (like FDA or ISO 13485), and prototyping tools is typically required. Strong problem-solving, collaboration, and self-motivation are vital soft skills for effective innovation and remote teamwork. These skills ensure safe, compliant, and innovative device development, even when working outside a traditional office setting.
What job categories do people searching Remote R&D Engineer Medical Device jobs in Rutherford, NJ look for? The top searched job categories for Remote R&D Engineer Medical Device jobs in Rutherford, NJ are:
Remote R D Engineer Medical Device 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 14 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.