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Medical Device Research And Development Jobs (NOW HIRING)

Medical Device R&D Engineer

San Jose, CA ยท On-site

$115K - $175K/yr

Minimum 5 years of medical device R&D experience * Hands-on catheter prototyping and testing experience required * Experience working within ISO 13485 Design Controls required * Experience with ...

Medical Device R&D Engineer

San Jose, CA ยท On-site

$115K - $175K/yr

Minimum 5 years of medical device R&D experience * Hands-on catheter prototyping and testing experience required * Experience working within ISO 13485 Design Controls required * Experience with ...

Senior Medical Device R&D Engineer

San Jose, CA ยท On-site

$150K - $225K/yr

Position Summary We are seeking a highly motivated, hands-on Senior Medical Device R&D Engineer to support the design, development, prototyping, testing, and manufacturing transfer of interventional ...

Senior Medical Device R&D Engineer

San Jose, CA ยท On-site

$150K - $225K/yr

Position Summary We are seeking a highly motivated, hands-on Senior Medical Device R&D Engineer to support the design, development, prototyping, testing, and manufacturing transfer of interventional ...

Minimum 5 years of medical device R&D experience * Hands-on catheter prototyping and testing experience required * Experience working within ISO 13485 Design Controls required * Experience with ...

Lead CdTe photovoltaic absorber research and development. * Develop and deploy new manufacturable ... D.) in a Device Development, Process Integration, or Process Development. * Semiconductor / Thin ...

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Medical Device Research And Development information

See salary details

$48.5K

$101.8K

$165K

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

As of Jun 21, 2026, the average yearly pay for medical device research and development in the United States is $101,794.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,500.00 and $116,500.00 per year, depending on experience, location, and employer.

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

To thrive in Medical Device Research and Development, you need a solid background in engineering or life sciences, along with experience in product design and knowledge of regulatory standards. Familiarity with CAD software, prototyping tools, and compliance systems such as ISO 13485 or FDA regulations is typically required. Strong problem-solving skills, creativity, and effective teamwork set standout professionals apart in this field. These skills and qualities are crucial to ensure innovative, safe, and compliant medical devices that meet both clinical needs and regulatory requirements.

What are some typical challenges faced by professionals in Medical Device Research and Development, and how can these be managed?

Professionals in Medical Device Research and Development often encounter challenges such as navigating complex regulatory requirements, balancing innovation with safety, and coordinating cross-functional teams. Managing these challenges involves staying current with FDA and international regulations, fostering open communication between engineering, clinical, and regulatory teams, and maintaining rigorous documentation throughout the development process. Strong project management skills and a collaborative mindset are key to overcoming these obstacles and ensuring successful product development.

What is medical device research and development?

Medical device research and development (R&D) is the process of designing, creating, testing, and improving medical devices used for diagnosing, treating, or preventing health conditions. This field combines engineering, biology, and medicine to develop innovative tools ranging from simple instruments to complex implantable devices. Professionals in this area work on everything from concept development and prototyping to clinical trials and regulatory approval. Their work ensures that medical devices are safe, effective, and meet strict regulatory standards before reaching patients.

What is the difference between Medical Device Research And Development vs Medical Device Quality Assurance?

AspectMedical Device Research And DevelopmentMedical Device Quality Assurance
CredentialsEngineering degrees, certifications in R&DQuality certifications, regulatory training
Work EnvironmentLabs, design teams, product developmentInspection facilities, compliance departments
Employer & Industry UsageManufacturers, biotech firms, innovation labsRegulatory agencies, manufacturing companies
Search & Comparison IntentInnovation, product development, prototypingCompliance, testing, product validation

Medical Device Research And Development focuses on designing and developing new medical devices, emphasizing innovation and prototyping. In contrast, Medical Device Quality Assurance ensures products meet safety and regulatory standards through testing and compliance. Both roles are essential in the medical device industry but serve different stages of the product lifecycle.

More about Medical Device Research And Development jobs
What cities are hiring for Medical Device Research And Development jobs? Cities with the most Medical Device Research And Development job openings:
What states have the most Medical Device Research And Development jobs? States with the most job openings for Medical Device Research And Development jobs include:
What job categories do people searching Medical Device Research And Development jobs look for? The top searched job categories for Medical Device Research And Development jobs are:
Infographic showing various Medical Device Research And Development job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 96% Full Time, 1% Part Time, and 2% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $101,794 per year, or $48.9 per hour.

Medical Device R&D Engineer

AngioSafe

San Jose, CA โ€ข On-site

$115K - $175K/yr

Full-time

Posted 22 days ago


Job description

AngioSafe is a Bay Area start-up focused on improving healthcare through state-of-the-art vascular interventional catheter device design, development, and manufacturing. We are pioneering the development of novel treatment mechanisms and algorithms to provide unprecedented access to peripheral and coronary disease treatments. Our experienced team is committed to developing and commercializing innovative, high-quality products that reduce risk and improve cardiovascular treatment outcomes. This onsite role will have a meaningful and direct impact on AngioSafe's device portfolio through the development of novel vascular interventional devices and support of existing product pipelines. The ideal candidate will combine strong engineering fundamentals with hands-on technical ability and thrive in a fast-paced startup environment.
Position Summary
We are seeking a highly motivated, hands-on Individual Contributor (IC) R&D Engineer to support the design, development, prototyping, testing, and manufacturing transfer of interventional catheter devices.This role is ideal for someone who enjoys building and testing devices directly, solving technical challenges, and working collaboratively within a small, rapidly evolving medical device company.
Roles and Responsibilities
  • Contribute to the design, development, testing, and manufacturing transfer of interventional catheter devices
  • Support development activities for both new and existing products
  • Perform hands-on prototyping, assembly, troubleshooting, and testing of medical devices
  • Generate technical documentation in accordance with Design Control requirements
  • Develop test methods, protocols, and reports for:
    • concept evaluations
    • verification & validation testing
    • component qualification
    • packaging and shelf-life validation
  • Support creation and maintenance of:
    • Bills of Materials (BOMs)
    • manufacturing process instructions
    • engineering specifications
    • risk management documentation
  • Work closely with suppliers to support component development and resolve non-conformance issues
  • Assist in maintaining shared laboratory and prototype spaces
  • Collaborate cross-functionally with engineering, manufacturing, quality, and leadership teams

Minimum Qualifications
  • 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 required
  • Experience working within ISO 13485 Design Controls required
  • Experience with document control systems and engineering change documentation
  • Strong hands-on engineering and troubleshooting abilities
  • Startup and/or small-company experience preferred
  • Proficiency with SolidWorks including:
    • 3D component and assembly modeling
    • 2D drawings per ASME Y14.5
  • Knowledge of catheter manufacturing materials and processes including:
    • braiding
    • lamination
    • laser welding
    • adhesive bonding
    • packaging
  • Strong communication and technical writing skills
  • Ability to manage multiple priorities in a fast-paced environment
  • Self-motivated with strong ownership mentality

Preferred Qualifications
  • Catheter design and development experience strongly preferred
  • Experience supporting FDA and/or Notified Body submissions
  • Experience using cloud-based document control systems
  • Project leadership experience preferred

Additional Information
  • This is a fully onsite role based in San Jose, CA
  • No relocation or immigration sponsorship available
  • Principals only please

Equal Opportunity Employer
AngioSafe is committed to a diverse workplace and is committed to equal opportunity employment for all job applicants without regard to race, color, religion, sex, sexual orientation, age, gender, gender identity or expression, size, national origin, disability, or veteran status. AngioSafe complies with all applicable local, state, and national laws governing non-discrimination in employment