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Medical Device Physician Jobs in Riverside, CA (NOW HIRING)

Cypress HCM

Control Systems Engineer

Irvine, CA · On-site

$200K - $250K/yr

A top medical device client is seeking a highly experienced, direct hire Control Systems Engineer ... physician collaborators and principal investigators. Salary of $200,000 to $250,000 annually ...

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All JobsMedical Device Physician JobsMedical Device Physician Jobs in Riverside, CA

Medical Device Physician information

See Riverside, CA salary details

$101.7K

$226.9K

$365.1K

How much do medical device physician jobs pay per year?

As of Sep 4, 2026, the average yearly pay for medical device physician in Riverside, CA is $226,853.00, according to ZipRecruiter salary data. Most workers in this role earn between $198,200.00 and $255,100.00 per year, depending on experience, location, and employer.

What is a medical device physician?

A Medical Device Physician is a licensed medical doctor who specializes in evaluating, developing, and overseeing the use of medical devices in healthcare settings. They collaborate with engineers, regulatory agencies, and clinical teams to ensure that medical devices are safe, effective, and compliant with regulations. Medical Device Physicians may be involved in clinical trials, post-market surveillance, and providing expert guidance in the design and improvement of medical devices. They play a crucial role in bridging the gap between clinical practice and medical technology innovation.

What are the key skills and qualifications needed to thrive as a medical device physician, and why are they important?

To thrive as a Medical Device Physician, you need a medical degree (MD or DO), board certification, and deep knowledge of clinical practices and regulatory standards for medical devices. Familiarity with clinical trial design, FDA regulations, and proficiency in using electronic data capture (EDC) systems are typically required. Strong communication, critical thinking, and collaborative skills help in liaising between clinical teams, regulatory bodies, and device manufacturers. These skills are crucial to ensure medical devices are safe, effective, and compliant with regulations, ultimately supporting patient safety and innovation.

How does a medical device physician typically collaborate with regulatory and engineering teams during product development?

Medical Device Physicians play a pivotal role in bridging the gap between clinical needs and technical solutions. They work closely with engineering teams to ensure device designs meet clinical requirements and with regulatory teams to facilitate compliance with safety and efficacy standards. Regular interdisciplinary meetings, reviewing technical documentation, and providing medical insights are common parts of their weekly responsibilities. This collaboration ensures that the final product is both clinically effective and meets all regulatory guidelines.

What is the difference between Medical Device Physician vs Medical Device Engineer?

AspectMedical Device PhysicianMedical Device Engineer
Required CredentialsMedical degree, medical license, specialized training in medical devicesBachelor's or master's in engineering, biomedical engineering, or related field
Work EnvironmentHospitals, clinics, regulatory agencies, medical device companiesResearch labs, manufacturing facilities, R&D departments
Employer & Industry UsageHealthcare providers, medical device companies, regulatory bodiesMedical device manufacturing, biotech firms, R&D organizations
Common Search & Comparison IntentUnderstanding clinical roles, regulatory responsibilities, medical expertiseDesign, development, testing of medical devices, technical engineering skills

The main difference is that Medical Device Physicians focus on clinical application, patient safety, and regulatory compliance, leveraging medical expertise. Medical Device Engineers concentrate on designing, developing, and testing medical devices using engineering principles. Both roles are essential in the medical device industry but serve different functions within the product lifecycle.

Is a medical device physician job in high demand?

Medical device physicians, who specialize in the clinical evaluation and approval of medical devices, are in increasing demand due to the growing medical technology industry and regulatory requirements. Their expertise is valuable in product development, regulatory submissions, and post-market surveillance, making the role relatively stable with good job prospects.

What are popular job titles related to Medical Device Physician jobs in Riverside, CA?

For Medical Device Physician jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Medical Device Physician jobs in Riverside, CA look for?

The top searched job categories for Medical Device Physician jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Medical Device Physician jobs?

Cities near Riverside, CA with the most Medical Device Physician job openings:

Medical Device Physician jobs near you
Infographic showing various Medical Device Physician job openings in Riverside, CA as of August 2026, with employment types broken down into 90% Full Time, 5% Part Time, and 5% Contract. Highlights an 84% In-person, and 16% Remote job distribution, with an average salary of $226,853 per year, or $109.1 per hour.

Senior Specialist, Clinical Education, Clinical Development

Edwards Lifesciences Corporation

Irvine, CA • On-site

$134K - $190K/yr

Full-time

Re-posted 29 days ago

Key responsibilities

  • Support the advancement of transcatheter therapies through hands-on clinical engagement, procedural innovation, and continuous learning.

  • Represent TMTT during complex research cases by providing on-site, real-time guidance during device implants and supporting procedural observations and issue escalation.

  • Develop educational materials and training on device handling, implantation, troubleshooting, and clinical imaging techniques related to device procedures.

Edwards Lifesciences rating

8.2

Company rating: 8.2 out of 10

Based on 31 frontline employees who took The Breakroom Quiz

86th of 545 rated manufacturers

Job description

Patients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs.It'sour driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.

How you'll make an impact:

  • The Senior Specialist, Clinical Development serves as a subject matter expert (SME) supporting the advancement of transcatheter therapies through hands-on clinical engagement, procedural innovation, and continuous learning. This role partners cross-functionally with physicians, R&D, and commercial teams to support complex cases, develop procedural techniques, and translate real-world clinical insights into next-generation device and therapy improvements.
  • Represent TMTT during complex research cases (ESAPCU, clinical trial, commercial) with investigating physicians, hospital staff and clinical research coordinators by providing on-site, real-time guidance during implants, including contingency planning to address unforeseen occurrences in support novel devices
  • Document procedural case observations for insights in investigating post procedural events. Support enrollment discussions and assistance with issue escalation with Principal Investigator and research team
  • Develop materials and provide education on all aspects of the device, device handling, implantation and troubleshooting techniques related to equipment, tools and products required for device implants.
  • Develop, analyze, and optimize the design of complex procedures, testing, and therapies leveraging substantial understanding of clinical imaging. Coordinate all clinical imaging training and instruction for cross-functional teams as products move from ESAPCU to early human use to the commercial setting. Create complex design control and trial-related documentation and support all complaint and investigational analyses supporting the therapy. Make recommendations for improvements
  • This position is on site in Irvine, Ca Full time with up to 50% travel nationwide

What you'll need (Required):

  • Bachelor's Degree in Engineering or Scientific field , 4 years experience including either industry or industry/education Required or

  • Master's Degree or equivalent in Engineering or Scientific field, 3 years experience including either industry or industry/education Required or

What else we look for (Preferred):

  • Demonstrated experience in customer-facing roles, including direct engagement with physicians and leading training and procedures on procedural execution and best practices
  • Substantial knowledge and understanding of principles, theories, and concepts relevant to Engineering and cardiovascular scienc
  • Full knowledge of cardiovascular anatomy, pathology, and physiology
  • Strong problem-solving, organizational, analytical, and critical thinking skills
  • Substantial understanding of medical device regulatory requirements and documents, adverse events reporting
  • Good leadership skills and ability to influence change; acts as a resource for colleagues with less experience
  • Strong documentation, communication (e.g., written and verbal) and interpersonal relationship skills including consultative and relationship management skills
  • Basic understanding of statistical techniques
  • Previous experience working with lab preferred
  • Knowledge of and adherence to Edwards Environmental Health and Safety and Quality guidelines as they relate to department clean room medical device manufacturing
  • proven expertise in Microsoft Office Suite including Word, PowerPoint, Access, and Excel
  • Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control

Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California (CA), the base pay range for this position is $134,000 to $190,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience).Applications will be accepted while this position is posted on our Careers website.


Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.

What Edwards Lifesciences employees say

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About Edwards Lifesciences

Sourced by ZipRecruiter

Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world's leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 15,000 individuals worldwide. For us, helping patients is not a slogan - it's our life's work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Irvine, CA, US

Year founded

1958

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