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Medical Device Product Development Manager Jobs (NOW HIRING)

Masimo

Manager, OEM Product Development

Irvine, CA · On-site

$135K - $170K/yr

The Manager, OEM Product Development leads a mission-critical engineering function responsible for ... Minimum of five (5) years of experience in medical device product development, systems engineering ...

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Medical Device Product Development Manager information

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$144.5K

How much do medical device product development manager jobs pay per year?

As of Jun 10, 2026, the average yearly pay for medical device product development manager in the United States is $126,987.00, according to ZipRecruiter salary data. Most workers in this role earn between $114,500.00 and $143,000.00 per year, depending on experience, location, and employer.

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

To thrive as a Medical Device Product Development Manager, you need expertise in engineering or life sciences, experience with product lifecycle management, and knowledge of regulatory requirements, often supported by a relevant degree. Familiarity with CAD software, project management tools, and compliance systems such as ISO 13485 or FDA regulations is typically required. Strong leadership, cross-functional communication, and problem-solving skills help drive innovation and align diverse teams. These competencies are vital to ensure products are developed efficiently, safely, and in compliance with industry standards.

How does a Medical Device Product Development Manager typically collaborate with cross-functional teams during the development process?

A Medical Device Product Development Manager works closely with cross-functional teams, including engineering, regulatory affairs, quality assurance, marketing, and clinical experts, to ensure that product requirements are met throughout each development phase. They facilitate regular meetings to align on project milestones, address potential risks, and incorporate feedback from various stakeholders. This collaborative environment helps ensure that the final product complies with regulatory standards and meets market needs, making strong communication and project management skills essential in this role.

What is the difference between Medical Device Product Development Manager vs Medical Device Quality Assurance Specialist?

AspectMedical Device Product Development ManagerMedical Device Quality Assurance Specialist
CredentialsEngineering degree, certifications like PMP or PDMAQuality assurance certifications like CQE, ISO auditor
Work EnvironmentDesign teams, R&D, cross-functional project groupsQuality labs, compliance departments, manufacturing oversight
Industry UsageLeading product development from concept to launchEnsuring products meet quality and regulatory standards

The Medical Device Product Development Manager focuses on designing and developing new medical devices, managing cross-functional teams, and bringing products to market. In contrast, the Medical Device Quality Assurance Specialist ensures that products meet quality standards and regulatory requirements throughout the development and manufacturing process. Both roles are essential in the medical device industry but serve different functions in product lifecycle management.

What does a Medical Device Product Development Manager do?

A Medical Device Product Development Manager oversees the entire process of bringing a medical device from the concept stage to market launch. They coordinate cross-functional teams, manage timelines, ensure compliance with regulatory standards, and oversee testing and validation of products. Their responsibilities also include working with engineers, designers, and regulatory specialists to ensure the device meets safety, efficacy, and user needs. Ultimately, they play a critical role in ensuring that new medical devices are developed efficiently, safely, and in compliance with industry standards.
What cities are hiring for Medical Device Product Development Manager jobs? Cities with the most Medical Device Product Development Manager job openings:
What are the most commonly searched types of Medical Device Product Development jobs? The most popular types of Medical Device Product Development jobs are:
What states have the most Medical Device Product Development Manager jobs? States with the most job openings for Medical Device Product Development Manager jobs include:
Medical Device Product Development Manager jobs near you
Infographic showing various Medical Device Product Development Manager job openings in the United States as of June 2026, with employment types broken down into 1% Locum Tenens, 84% Full Time, and 15% Part Time. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $126,987 per year, or $61.1 per hour.
Manager, OEM Product Development

Manager, OEM Product Development

Masimo

Irvine, CA • On-site

$135K - $170K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 17 days ago

Job description

Job Description
Job Summary:
The Manager, OEM Product Development leads a mission-critical engineering function responsible for the design, development, and integration of Masimo technologies within OEM partner platforms. This role manages a team of engineers and technical contributors supporting OEM product development activities, including requirements definition, system integration, verification, and lifecycle support. The Manager ensures technical execution aligns with Masimo's product roadmap, quality standards, and regulatory requirements while enabling successful OEM product launches and sustainment.
Duties & Responsibilities:
  • Lead and manage OEM product development activities supporting the integration of Masimo technologies into OEM partner platforms, from concept through launch and sustainment.
  • Provide technical leadership for OEM product introductions, including architecture reviews, design discussions, and technical enablement with OEM engineering teams.
  • Own OEM technical integration efforts for Masimo SET and Rainbow SET technologies, coordinating cross-functionally with Engineering, Quality, Regulatory, Manufacturing, and Operations teams.
  • Support OEM product upgrades and change initiatives by leading engineering execution, risk assessment, and validation activities.
  • Represent OEM Product Development in technical forums, design reviews, and partner working sessions as needed.
  • Contribute to OEM product strategy and roadmap planning through technical feasibility analysis, risk evaluation, and cross-functional collaboration.
  • Lead continuous improvement initiatives to enhance OEM development processes, design controls, and cross-functional execution.
  • Manage, coach, and develop direct reports; set technical priorities, allocate resources, conduct performance reviews, and build organizational capability within OEM Product Development.

Minimum Qualifications:
  • Minimum of five (5) years of experience in medical device product development, systems engineering, or OEM integration, with demonstrated experience supporting complex hardware and/or software products
  • Demonstrated experience leading and developing engineering or technical teams with accountability for execution and delivery
  • Working knowledge of FDA and international regulatory requirements, including design controls and product development lifecycle expectations
  • Strong organizational, planning, and analytical skills; ability to manage multiple development programs concurrently
  • Excellent communication skills with the ability to translate complex technical concepts to cross-functional and external stakeholders
  • Ability to exercise independent technical judgment, manage competing development priorities, and travel as business needs require
  • Experience operating effectively in both structured and fast-paced development environments
  • Demonstrated adaptability and problem-solving skills in dynamic engineering environments
  • Ability to work onsite Monday-Friday in Irvine, CA.

Preferred Qualifications:
  • Experience with OEM or partner-integrated medical device development
  • Systems engineering, electrical, mechanical, or software engineering background
  • Prior experience leading cross-functional development teams

Education:
Bachelor's degree in engineering or a related technical discipline required. Advanced degree preferred.
Compensation:
The anticipated range for this position is $135k - $170k. Actual placement within the range is dependent on multiple factors, including but not limited to skills, education, and experience. Masimo offers benefits such as Medical, Dental, Vision, Life/AD&D, Disability Insurance, 401(k), Vacation, Sick, Holiday, Paid Maternity Leave, Flexible Spending Accounts, voluntary Accident, Critical Illness, Hospital, Long-Term Care, Employee Assistance Program, Pet Insurance, on-site Wellness Clinic, Fitness Center, Café. All benefits are subject to eligibility requirements.
Physical requirements/Work Environment:
This position primarily works in an office environment. It requires frequent sitting, standing and walking. Daily use of a computer and other computing and digital devices is required. May stand for extended periods when facilitating meetings or walking in the facilities. Some travel may be necessary.
The physical demands of the position described herein are essential functions of the job and employees must be able to successfully perform these tasks for extended periods. Reasonable accommodations may be made for those individuals with real or perceived disabilities to perform the essential functions of the job described.
Masimo is proud to be an EOE/, M/F/D/V, and we are committed to Diversity at every level
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About Masimo

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Irvine, CA, US

Year founded

1989

Social media

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