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Medical Device Program Manager Jobs in Springfield, MA

Encompass Health

Dialysis Program Manager

Ludlow, MA · On-site

Area Dialysis Program Manager Career Opportunity Recognized for your expertise as an Area Dialysis ... Affordable medical, dental, and vision plans for both full-time and part-time employees and their ...

Viant

Director of Operations

Brimfield, MA · On-site

$180 - $210K/hr

About the company: Viant is a global medical device partner providing design, development ... Oversees and manages the activities of: production, engineering, warehouse/inventory management

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

Medical Device Program Manager information

See Springfield, MA salary details

$38.4K

$107.1K

$156.4K

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

As of Jul 14, 2026, the average yearly pay for medical device program manager in Springfield, MA is $107,085.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,200.00 and $132,000.00 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 are popular job titles related to Medical Device Program Manager jobs in Springfield, MA? For Medical Device Program Manager jobs in Springfield, MA, the most frequently searched job titles are:
What job categories do people searching Medical Device Program Manager jobs in Springfield, MA look for? The top searched job categories for Medical Device Program Manager jobs in Springfield, MA are:
What cities near Springfield, MA are hiring for Medical Device Program Manager jobs? Cities near Springfield, MA with the most Medical Device Program Manager job openings:
Medical Device Program Manager jobs near you
QA Strategy Lead - Medical Devices & Compliance

QA Strategy Lead - Medical Devices & Compliance

Merck

Hartford, CT • On-site

$142K - $224K/yr

Full-time

This job post has expired today. Applications are no longer accepted.

Merck rating

7.8

Company rating: 7.8 out of 10

Based on 50 frontline employees who took The Breakroom Quiz

44th of 74 rated pharmaceutical

Job description

Merck is seeking an Associate Director Quality Engineering & Quality Assurance in Hartford, CT to oversee compliance related to medical devices and Combination Products. This role demands a minimum of 7 years in quality assurance and regulatory affairs within the medical device industry.

The ideal candidate will have expertise in device regulations, design controls, and risk management. Benefits include a substantial salary range of $142,400 – $224,100 and eligibility for bonuses.

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