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Director Medical Device Product Development information

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$73K

$163.7K

$244.5K

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

As of Jun 30, 2026, the average yearly pay for director medical device product development in the United States is $163,684.00, according to ZipRecruiter salary data. Most workers in this role earn between $131,500.00 and $185,500.00 per year, depending on experience, location, and employer.

What is the difference between Director Medical Device Product Development vs Product Manager Medical Devices?

AspectDirector Medical Device Product DevelopmentProduct Manager Medical Devices
ResponsibilitiesOversees entire product development lifecycle, manages teams, sets strategic directionFocuses on product planning, feature definition, and market analysis
Required CredentialsEngineering or life sciences degree, experience in medical device development, regulatory knowledgeBackground in engineering, marketing, or life sciences, familiarity with medical device regulations
Work EnvironmentLeadership role in R&D or product development departments, cross-functional teamsCollaborates with engineering, marketing, and sales teams, often in a more tactical role

The main difference is that the Director Medical Device Product Development leads and manages the entire development process and teams, focusing on strategic oversight, while the Product Manager Medical Devices concentrates on product planning and market needs. The director role involves higher-level management and regulatory oversight, whereas the product manager handles day-to-day product features and customer requirements.

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Director Medical Device Product Development jobs near you
Product development Engineer(Medical device)

Product development Engineer(Medical device)

Intellectt INC

Foxboro, MA • On-site

Contractor

Posted 3 days ago

Job description

Role : Product development Engineer
Location:Mansfield, MA 
 
Job description:

  • Contribute to medical device product development and sustaining activities

  • Draft test protocols, perform data analysis, and ensure traceability to requirements

  • Participate in design verification & validation (V&V) efforts

  • Support EUMDR remediation projects and update technical documentation

  • Collaborate with cross-functional teams to ensure compliance with regulatory standards

  • Work with technical files, risk management documentation, and design history files (DHF)

Must-Have Qualifications:

  • Bachelor’s degree in Engineering (Mechanical or Biomedical preferred)

  • 5+ years of medical device industry experience

  • 3+ years in product development or R&D

  • Strong understanding of design controls, V&V process, and traceability