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Medical Device Program Manager Jobs in Sutton, MA

... medical device programs Key Responsibilities * Lead all site supply chain activities, including ... Manage and develop a team of direct reports while providing leadership across broader cross ...

... management • Execution of system and subsystem verification testing • Drive continuous ... electromechanical medical device programs through the verification and validation phases • ...

Senior Systems Test Engineer

Newton, MA · On-site

$115K - $157K/yr

... management • Execution of system and subsystem verification testing • Drive continuous ... electromechanical medical device programs through the verification and validation phases • ...

... management • Execution of system and subsystem verification testing • Drive continuous ... electromechanical medical device programs through the verification and validation phases • ...

... management • Execution of system and subsystem verification testing • Drive continuous ... electromechanical medical device programs through the verification and validation phases • ...

Program Manager

Boston, MA · On-site

$53K - $77K/yr

... the Program Manager will lead the design, implementation, and evaluation of longitudinal ... Medical Center and Boston University Medical Campus. Reporting to the Director of Faculty ...

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Showing results 1-20

Medical Device Program Manager information

See Sutton, MA salary details

$40.2K

$112.3K

$164.1K

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

As of Jul 15, 2026, the average yearly pay for medical device program manager in Sutton, MA is $112,322.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,100.00 and $138,500.00 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 cities near Sutton, MA are hiring for Medical Device Program Manager jobs? Cities near Sutton, MA with the most Medical Device Program Manager job openings:
Medical Device Manufacturing Engineer (Capital Equipment)

Medical Device Manufacturing Engineer (Capital Equipment)

IPG Photonics

Marlborough, MA

$75K - $97K/yr

Full-time

Re-posted 10 days ago


IPG Photonics rating

8.2

Company rating: 8.2 out of 10

Based on 18 frontline employees who took The Breakroom Quiz

106th of 430 rated machine equipment manufacturers


Job description

IPG Photonics is revolutionizing the laser industry as the pioneering developer and leading producer of fiber lasers and amplifiers. Headquartered in Marlborough, MA, IPG has over 4,800 employees in more than 30 locations around the world. We aspire to work together with our employees and customers to apply light in ways that improve life.

Our mission is to develop innovative laser solutions to make the world a better place. To accomplish this mission, we are committed to attracting and retaining the best talent and an engaged and thriving workforce that drives a sustainable future for our company and society.

Working at IPG Photonics you can expect challenging projects, a motivating and friendly environment, and competitive benefits.

Job Summary

The Manufacturing Engineer is responsible for supporting the manufacture and service of medical devices and disposables. This role focuses on production workflow optimization, documentation, tooling development, regulatory compliance, and cross-functional collaboration to ensure efficient, compliant, and repeatable manufacturing operations.

This position is governed by the IPG Medical Corporation Quality Management System and applicable regulatory and quality standards.

Job Functions

  • Organizes production workflow to maximize efficiency and contain total costs of assembly.
  • Develops, approves, and reviews work instructions and test procedures to support standardized work in the production area.
  • Develops and qualifies tooling to improve manufacturing process yield and reduce process variation.
  • Conducts training for production and quality associates.
  • Assists with planning, scheduling, and coordination of production activities to fulfill customer orders.
  • Executes production process transactions using the ERP system.
  • Ensures compliance of the production environment with cGMP, ISO, and all other applicable medical device standards and regulations.
  • Initiates and executes disposition of NonConforming Material Reports (NCMRs); assists with investigation of productionrelated CAPAs.
  • Works with engineering to feedback design issues and resolve them for future builds through the ECO system.
  • Participates in new vendor qualification activities to improve supplier performance.
  • Evaluates alternate sources for BOM components and makes recommendations to design engineering.
  • Initiates process control improvements to support cost reduction and ontime delivery objectives.
  • Participates in service and repair of customerowned and remanufactured equipment.
  • Develops and executes experiments to test new components and manufacturing processes prior to product use.

Requirements

Education

  • Bachelor of Science degree in a technical discipline or equivalent work experience.
  • Strong knowledge of U.S. and global regulatory requirements for medical devices.
  • Solid project management skills.
  • Knowledge of the Russian language is preferred but not required.

Experience

  • 3-5+ years of experience in the manufacture and service of medical device equipment
  • Disposable medical device a plus
  • Laser experience a plus
  • Proficient in the use of test equipment such as digital voltmeters, oscilloscopes, and laboratory power supplies.
  • Proficient with light manufacturing and assembly equipment, including PCB soldering stations and wire cutting/stripping tools.
  • Working knowledge of ERP systems and Microsoft Office applications.

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  • Education

    • Bachelor of Science degree in a technical discipline or equivalent work experience.
    • Strong knowledge of U.S. and global regulatory requirements for medical devices.
    • Solid project management skills.
    • Knowledge of the Russian language is preferred but not required.

    Experience

    • 3-5+ years of experience in the manufacture and service of medical device equipment
    • Disposable medical device a plus
    • Laser experience a plus
    • Proficient in the use of test equipment such as digital voltmeters, oscilloscopes, and laboratory power supplies.
    • Proficient with light manufacturing and assembly equipment, including PCB soldering stations and wire cutting/stripping tools.
    • Working knowledge of ERP systems and Microsoft Office applications.

What IPG Photonics employees say

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