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Research Development Medical Device Engineer Jobs

... • Oversee R&D technician's work including testing and prototype assembly • Generate new or ... years of Medical Device R&D experience o Working within ISO 13485 regulated Design Controls o ...

Device Engineer III

Foster City, CA · On-site

$117K - $152K/yr

We are seeking a highly skilled and proactive Device Engineer III to support testing, method development, design verification and method transfer activities for medical devices and parenteral ...

Device Engineer III

Foster City, CA · On-site

$117K - $152K/yr

We are seeking a highly skilled and proactive Device Engineer III to support testing, method development, design verification and method transfer activities for medical devices and parenteral ...

Bachelor's degree in Mechanical Engineering or related engineering discipline preferred * Minimum 5 years of medical device R&D experience * Hands-on catheter prototyping and testing experience ...

Sr Medical Device Engineer

San Diego, CA · On-site

$110K - $152K/yr

Cpk, ANOVA, T-Test, MSA, GR&R, DOE You will work with vendors & diverse engineering teams to ... an R&D environment. What you'll get: * A front row seat to life changing CGM technology. Learn ...

Senior Device Engineer

Maryland Heights, MO · On-site

$101K - $138K/yr

Liaison with internal production sites, quality, regulatory R&D, and Tech Transfer/Launch Teams ... Experience in Medical Device or Combination Products Design Controls, Production, Sustaining ...

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Research Development Medical Device Engineer information

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$20K

$96.6K

$151K

How much do research development medical device engineer jobs pay per year?

As of Jun 5, 2026, the average yearly pay for research development medical device engineer in the United States is $96,571.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,500.00 and $117,000.00 per year, depending on experience, location, and employer.

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

To thrive as a Research Development Medical Device Engineer, you need a strong background in biomedical engineering, mechanical or electrical engineering, and experience with product development processes, usually supported by a relevant degree. Familiarity with CAD software, prototyping tools, regulatory standards such as ISO 13485, and potentially Six Sigma or similar certifications is important. Creativity, analytical thinking, and effective teamwork skills help drive innovation and solve complex engineering challenges in multidisciplinary environments. These skills and qualifications are vital to ensure medical devices are safe, effective, and compliant with industry regulations while meeting user and market needs.

What are some typical challenges faced by Research Development Medical Device Engineers when bringing a new device from concept to prototype?

Research Development Medical Device Engineers often encounter challenges such as navigating strict regulatory requirements, coordinating with cross-functional teams, and balancing innovation with manufacturability. Ensuring the device meets safety and efficacy standards while staying within budget and timeline constraints can be demanding. Additionally, effective collaboration with clinicians, quality assurance, and manufacturing teams is crucial to address technical hurdles and incorporate user feedback throughout the development process.

What does a Research Development Medical Device Engineer do?

A Research Development Medical Device Engineer is responsible for designing, developing, and testing new medical devices or improving existing ones. They work closely with cross-functional teams, including clinicians, regulatory specialists, and manufacturing engineers, to ensure that devices are safe, effective, and compliant with industry standards. Their work involves prototyping, conducting experiments, analyzing data, and documenting results throughout the product development lifecycle. Additionally, they may help navigate regulatory approval processes and support product launches.

What is the difference between Research Development Medical Device Engineer vs Product Development Engineer?

AspectResearch Development Medical Device EngineerProduct Development Engineer
CredentialsBachelor's or Master's in Engineering, Biomedical, or related fields; certifications varyBachelor's or Master's in Engineering, Mechanical, Electrical, or related fields; certifications vary
Work EnvironmentResearch labs, R&D departments, clinical settingsManufacturing, design teams, product testing facilities
Employer & Industry UsageMedical device companies, biotech firms, healthcare institutionsMedical device companies, tech firms, manufacturing industries

The Research Development Medical Device Engineer focuses on early-stage research, innovation, and prototype development of medical devices. In contrast, the Product Development Engineer emphasizes designing, testing, and refining products for manufacturing and market release. Both roles require technical expertise, but their focus and project stages differ significantly.

More about Research Development Medical Device Engineer jobs
What cities are hiring for Research Development Medical Device Engineer jobs? Cities with the most Research Development Medical Device Engineer job openings:
What states have the most Research Development Medical Device Engineer jobs? States with the most job openings for Research Development Medical Device Engineer jobs include:
Infographic showing various Research Development Medical Device Engineer job openings in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $96,571 per year, or $46.4 per hour.

Research and Development Project Manager

Weekday AI

San Clemente, CA • On-site

Full-time

Posted 4 days ago


Job description

This role is for one of the Weekday's clients
Now Hiring: Senior Project Manager - R&D Medical Device New Product Development
San Clemente, CA (Hybrid)
Competitive Salary Long-Term Role
Various shifts might be available, with compensation varying based on the selected shift.
We are currently looking for a seasoned Senior Project Manager with extensive experience in Medical Device New Product Development (NPD) to lead enterprise-level R&D projects within a highly regulated healthcare setting.
The successful candidate should possess practical expertise in managing products throughout the entire medical device development process - including design inputs, verification and validation, regulatory submissions, and product launch.
Requirements
Qualifications We Seek:
• Extensive experience in Medical Device New Product Development (NPD)
• In-depth knowledge of Design Controls
• Proven background in supporting FDA 510(k), MDR, and other regulatory submissions
• Capacity to perform effectively in fast-paced and ambiguous R&D settings
• Demonstrated track record of driving alignment across cross-functional teams including R&D, Regulatory, Quality, Operations, and Supply Chain
• Experience with supporting product launch and ongoing sustaining engineering efforts
Primary Responsibilities:
• Lead complex R&D and New Product Development initiatives within FDA-regulated contexts
• Oversee project execution from initial concept through to commercialization
• Manage schedules, budgets, resources, risks, and deliverables associated with projects
• Coordinate multidisciplinary teams such as Regulatory Affairs, Quality, Manufacturing, Operations, Marketing, and Supply Chain
• Support design control activities, including product performance, assembly integrity, safety, labeling, packaging, as well as verification and validation tasks
• Collaborate with stakeholders to establish project scope, validation strategies, and requirements in dynamic development environments
• Ensure compliance of all projects with FDA, ISO 13485, GMP, and MDR standards
• Deliver executive-level project status updates and communications
Required Qualifications:
• Bachelor's degree mandatory
• Minimum of 4 years' experience in Project Management within Medical Device or regulated healthcare industries
• Experience in Design Controls and Medical Device Development Lifecycle
• Strong comprehension of NPD processes and regulatory frameworks
• Skilled in MS Project, Excel, PowerPoint, SharePoint, and other related project management tools
This role represents a fantastic opportunity for a self-driven individual who excels in early-stage product development and can lead execution across multiple teams independently.
Must-have skills
R&D medical device Medical Devices Medical Device R&D Biomedical Device Design Biomedical Devices