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Medical Device Program Manager Jobs in Needham, MA

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 ...

JRG Partners

Marketing Program Manager

Boston, MA · On-site

Marketing Programs Manager Status: Exempt Position: Reports to: Vice President, Marketing Our ... At least 5 years of experience in medical device or pharma companies * Skills: * Very comfortable ...

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

Medical Device Program Manager information

See Needham, MA salary details

$41.9K

$117.1K

$171K

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

As of Jul 16, 2026, the average yearly pay for medical device program manager in Needham, MA is $117,064.00, according to ZipRecruiter salary data. Most workers in this role earn between $86,600.00 and $144,300.00 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 Needham, MA look for? The top searched job categories for Medical Device Program Manager jobs in Needham, MA are:
What cities near Needham, MA are hiring for Medical Device Program Manager jobs? Cities near Needham, MA with the most Medical Device Program Manager job openings:
Medical Device Program Manager jobs near you
Infographic showing various Medical Device Program Manager job openings in Needham, MA as of July 2026, with employment types broken down into 86% Full Time, 7% Contract, and 7% Nights. Highlights an 65% In-person, 14% Hybrid, and 21% Remote job distribution, with an average salary of $117,064 per year, or $56.3 per hour.
Senior Manufacturing Quality Engineer (Medical Device)

Senior Manufacturing Quality Engineer (Medical Device)

Intellectt INC

Marlborough, MA • On-site

$91K - $124K/yr

Contractor

Posted 26 days ago

Job description

Hello,

I hope you're doing well.

My name is Mahalakshmi, and I’m reaching out from Intellectt Inc. regarding an exciting contract opportunity for a Senior Manufacturing Quality Engineer (Medical Device) based in Marlborough, MA, with one of our prestigious clients.
I would love to connect and discuss this opportunity in more detail. Please feel free to share your updated resume at mahalakshmi.n@intellectt.com  OR +1 (732) 737 8381
Job Title: Senior Manufacturing Quality Engineer (Medical Device)
Location: Marlborough, MA

Job Summary

Seeking a hands-on Senior Manufacturing Quality Engineer with 5+ years of experience in medical device manufacturing to support production and process quality activities. The role involves process validation, quality documentation, risk management, and collaboration with Manufacturing, Validation, and Operations teams to ensure compliant and efficient manufacturing processes.

Key Responsibilities

  • Provide daily quality engineering support for manufacturing operations.
  • Support production and process quality activities.
  • Lead and support Process Validation and TMV activities.
  • Develop and maintain PFMEA, CAPA, CPQ, and CTQ documentation.
  • Author and update protocols, reports, and quality documents.
  • Collaborate with Manufacturing Engineering, Validation, and Operations teams.
  • Troubleshoot quality issues and drive continuous improvement initiatives.

Required Qualifications

  • 5+ years of Quality Engineering experience in medical device manufacturing.
  • Strong background in production and process quality.
  • Experience with electromechanical medical devices.
  • Hands-on expertise in Process Validation, TMV, PFMEA, CAPA, and CPQ/CTQ.
  • Strong technical writing and documentation skills.
  • Ability to work on the manufacturing floor in a fast-paced environment.

Preferred Qualifications

  • Experience with IVD (In Vitro Diagnostics) products.
  • Familiarity with Agile PLM.

Ideal Candidate
Hands-on, execution-focused quality professional with strong problem-solving skills and the ability to work independently and cross-functionally in a regulated manufacturing environment.
Thanks & Regards,
Mahalakshmi
Junior Recruiter
Intellectt Inc 
mahalakshmi.n@intellectt.com
Direct: +1 (732) 737 8381