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Medical Device Product Development Manager Jobs (NOW HIRING)

Intellectt INC

R&D Engineer Human Factors

Milpitas, CA · On-site

Medical device product development experience * Knowledge of regulatory usability standards and ... Manager interview (may include technical discussion around usability and human factors experience)

Alexion Pharmaceuticals

$97K - $146K/yr

Understanding of medical device product development risk management methodologies. Possesses expertise in statistical analysis (Minitab, Crystal Ball, etc), analytical tools (e.g. FEA), benchtop ...

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Medical Device Product Development Manager information

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

As of Jul 21, 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 July 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. 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.
R&D Engineer Human Factors

R&D Engineer Human Factors

Intellectt INC

Milpitas, CA • On-site

Contractor

Posted 17 days ago

Job description

Role: R&D Engineer_Human Factors
Location: Milpitas, CA - 95035
Duration: 12 Months
Shift Timings: 8am-5pm
Work Mode:Onsite
Open to National Search:Yes (candidates must relocate if not local)
Looking for (Skills):
Human Factors / Usability Engineering professional with strong experience in user experience (UX), usability studies, and safety-focused product design, preferably in the medical device industry.
Must have Skills:
* Human Factors Engineering / Usability Engineering
* User Experience (UX) and usability testing
* Risk management and safety analysis
* Experience working in regulated environments (medical device preferred)
* Ability to conduct usability studies and user-centered design activities
Good to have skills:
* Experience working with hardware, software, and service systems
* Medical device product development experience
* Knowledge of regulatory usability standards and documentation
Day to day activity:
* Conduct and support human factors and usability engineering activities
* Perform usability studies and user research
* Analyze user interaction risks and safety considerations
* Collaborate with cross-functional R&D teamsduring product development
* Ensure products are designed with user safety and usability in mind
Education:
Bachelor’s or Master’s degree in Human Factors, Engineering, Psychology, Design, or related field
Experience:
Minimum 8+ years of relevant experience(10 years preferred) in human factors / usability engineering.
Interview:
Manager interview (may include technical discussion around usability and human factors experience).
Top skills:
* Human Factors Engineering
* Usability Engineering / UX
* Risk & Safety Analysis
* Medical Device Product Development