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Medical Device Program Manager Jobs in Mansfield, MA

Archimedic Inc

Program Manager

Waltham, MA

The Program Manager role leads technical medical device programs. This role reports to the Vice President, Program Managment & Quality. Essential Job Functions: * Program Management Activities:

Archimedic Inc

Senior Program Manager

Waltham, MA

$126K - $127K/yr

The Senior Program Manager role leads technical medical device programs while playing a role in product engineering. This role reports to the Vice President, Program Management & Quality. Essential ...

WHOOP

Senior Program Manager, SaMD

Boston, MA · On-site

$126K - $126K/yr

They are looking for a Senior Program Manager, SaMD to join their growing team and help scale the execution of their Software as a Medical Device programs, partnering with cross-functional leaders to ...

Whoop

Senior Program Manager, SaMD

Boston, MA · On-site

$155K - $185K/yr

We are looking for a Senior Program Manager, SaMD to join our growing team and help scale the execution of our Software as a Medical Device programs. This role will partner closely with an existing ...

Philips

Program Manager (Sustaining)

Cambridge, MA · On-site

$136K - $216K/yr

Owning the sustainment program management for a portfolio of medical devices, including hardware, Software as a Medical Device (SaMD), and connected digital platforms. Ensuring products in the field ...

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All JobsMedical Device Program JobsMedical Device Program Manager JobsMedical Device Program Manager Jobs in Mansfield, MA

Medical Device Program Manager information

See Mansfield, MA salary details

$40.8K

$113.8K

$166.2K

How much do medical device program manager jobs pay per year?

As of Aug 5, 2026, the average yearly pay for medical device program manager in Mansfield, MA is $113,758.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,200.00 and $140,300.00 per year, depending on experience, location, and employer.

What is the difference between Medical Device Program Manager vs Medical Device Quality Engineer?

AspectMedical Device Program ManagerMedical Device Quality Engineer
CredentialsProject management certifications, engineering degreeQuality assurance certifications (e.g., CQE), engineering degree
Work EnvironmentCross-functional teams, project planning, product developmentQuality systems, compliance, testing, and validation
Employer & Industry UsageMedical device companies, manufacturing, R&DRegulatory agencies, manufacturing, quality departments
Search & Comparison IntentManaging projects, product launches, timelinesEnsuring quality, compliance, risk management

The Medical Device Program Manager focuses on overseeing product development projects, coordinating teams, and ensuring timely delivery. In contrast, the Medical Device Quality Engineer concentrates on maintaining quality standards, regulatory compliance, and testing processes. Both roles are essential in the medical device industry but serve different functions within the product lifecycle.

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

To thrive as a Medical Device Program Manager, you need a strong background in project management, regulatory compliance, and biomedical engineering or a related field, often supported by a relevant degree and industry experience. Familiarity with project management tools (such as MS Project), quality management systems (QMS), and certifications like PMP or Six Sigma are highly valued. Exceptional leadership, cross-functional communication, and problem-solving skills help drive successful product development and team coordination. These competencies ensure programs meet regulatory standards, stay on schedule, and deliver safe, effective medical devices to market.

What is a medical device program manager?

A Medical Device Program Manager oversees the planning, development, and execution of projects related to medical devices within a company. They coordinate cross-functional teams, manage timelines, ensure regulatory compliance, and serve as the main point of contact for stakeholders. Their role is crucial in bringing safe and effective medical devices from concept to market, ensuring that all aspects of the program meet quality and regulatory standards. Medical Device Program Managers often work closely with engineering, quality assurance, regulatory affairs, and marketing teams.

How does a medical device program manager typically collaborate with cross-functional teams during product development?

A Medical Device Program Manager works closely with cross-functional teams including engineering, regulatory affairs, quality assurance, manufacturing, and marketing throughout the product development lifecycle. They coordinate timelines, facilitate communication, and resolve conflicts to ensure project milestones are met while maintaining compliance with regulatory standards. Regular meetings and progress updates are essential, as the Program Manager acts as a central point of contact to align various team goals and address issues proactively. This collaborative approach helps streamline development and supports successful product launches.
What job categories do people searching Medical Device Program Manager jobs in Mansfield, MA look for? The top searched job categories for Medical Device Program Manager jobs in Mansfield, MA are:
What cities near Mansfield, MA are hiring for Medical Device Program Manager jobs? Cities near Mansfield, MA with the most Medical Device Program Manager job openings:
Medical Device Program Manager jobs near you

Medical Device Test Engineer

Conflux Systems

Newton, MA • On-site

Full-time

Re-posted 27 days ago

Job description

We are seeking a Contract System Test Engineer to support verification activities for a complex medical robotics system used in advanced robotic-assisted vascular interventions. The role focuses on developing and executing system-level testing, ensuring product requirements traceability, and supporting verification and validation for complex electromechanical medical devices. The ideal candidate will contribute to quality processes, implement verification methods, and support continuous improvement across systems engineering and testing workflows.
Responsibilities:
  • Develop and implement test methods for verification of complex medical robotic systems.
  • Execute system and subsystem verification testing during verification and validation (V&V) phases.
  • Maintain and update requirements traceability and risk management documentation.
  • Implement processes within verification and issue management toolchains.
  • Perform statistical analysis and determine sample size for tests using statistical methods.
  • Validate software tools and test fixtures used in testing activities.
  • Support continuous improvement of systems engineering and quality processes.

Qualifications:
  • Bachelor's degree in Systems Engineering, Biomedical Engineering, Robotics, Software Engineering, Mechanical Engineering, or Electrical Engineering.
  • 5+ years of experience in medical device testing, preferably with medical or surgical robotics systems.
  • Strong knowledge of verification strategy development, test method validation, and requirements traceability.
  • Experience with IEC 60601-1 and related medical device standards.
  • Background in electromechanical systems testing, statistical test analysis, and verification toolchain implementation.
  • Experience supporting complex medical device programs through verification and validation phases.

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