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Medical Device Program Manager Jobs in New Hampshire

Invio Automation

Program Manager

Hudson, NH · On-site

... markets including medical device and life sciences, renewable energy, mobility, logistics ... Program Managers in Solutions play a crucial role in our organization, as they are responsible for ...

Invio Automation

Program Manager

Hudson, NH

... markets including medical device and life sciences, renewable energy, mobility, logistics amp ... Program Managers in Solutions play a crucial role in our organization, as they are responsible for ...

Emerald Technologies

Program Manager

Salem, NH · On-site

The Program Manager is a strategic project-management professional who works on customer projects ... Competitive medical, dental, and vision benefits  * Health Savings Account/Flexible Spending ...

Analogic

Program Manager

Salem, NH

Software Program Manager Make an Impact That Matters At Analogic, we don't just build technology ... Familiarity with regulated environments (e.g., medical devices, FDA 21 CFR Part 820) is a plus

Analogic Corporation

Program Manager

Salem, NH

Software Program Manager Make an Impact That Matters At Analogic, we don't just build technology ... Familiarity with regulated environments (e.g., medical devices, FDA 21 CFR Part 820) is a plus

Analogic

Program Manager

Salem, NH · On-site

Software Program Manager Make an Impact That Matters At Analogic, we don't just build technology ... Familiarity with regulated environments (e.g., medical devices, FDA 21 CFR Part 820) is a plus

Analogic

Program Manager

Salem, NH · On-site

They are seeking a Software Program Manager to lead software projects from concept through deployment, driving innovation across security and medical technology domains. Responsibilities : • Own ...

Community Options

Program Manager

Nashua, NH · On-site

$50K/yr

The Program Manager leads a team to provide person-centered care tailored to meet the needs of ... Monitor the health and medical needs of individuals and immediately report any concerns * Manage ...

Community options

Program Manager

Nashua, NH · On-site

$50K/yr

The Program Manager leads a team to provide person-centered care tailored to meet the needs of ... Monitor the health and medical needs of individuals and immediately report any concerns * Manage ...

Analogic Corporation

Program Manager

Salem, NH

Join our team as an Engineering Program Manager , where you'll lead complex, high-impact programs that power solutions in the medical and aviation security sectors. In this role, you won't just ...

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All JobsMedical Device Program JobsMedical Device Program Manager JobsMedical Device Program Manager Jobs in New Hampshire

Medical Device Program Manager information

See New Hampshire salary details

$37.4K

$104.5K

$152.7K

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

As of Aug 26, 2026, the average yearly pay for medical device program manager in New Hampshire is $104,506.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,300.00 and $128,900.00 per year, depending on experience, location, and employer.

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 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 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 popular job titles related to Medical Device Program Manager jobs in New Hampshire?

For Medical Device Program Manager jobs in New Hampshire, the most frequently searched job titles are:

What job categories do people searching Medical Device Program Manager jobs in New Hampshire look for?

The top searched job categories for Medical Device Program Manager jobs in New Hampshire are:

Medical Device Program Manager jobs near you
Infographic showing various Medical Device Program Manager job openings in New Hampshire as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, and 5% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $104,506 per year, or $50.2 per hour.

Agile Program Lead / Principal Software Engineer - Medical Device Development

Suntra MedTech Solutions

Bedford, NH • On-site

Full-time

Re-posted 15 days ago

Job description

Description

 We are accepting resumes for an experienced software engineer operating as a Product Owner / Scrum Master to serve as the connective tissue between technical development teams (software, firmware, systems, cybersecurity, electronics, mechanical, test) and the Program Manager responsible for overall product delivery. This role ensures that requirements are clearly defined, prioritized, and executed using agile practices-while maintaining compliance with medical device regulatory standards.

The ideal candidate understands both agile product delivery and regulated medical device development and can enable the team to benefit from an agile development process while ensuring that program-level objectives are met.


Responsibilities

Product Ownership & Backlog Management

  • Own and manage the product backlog, ensuring alignment with program milestones, regulatory requirements, and customer needs
  • Translate program-level requirements, system requirements, and user needs into clear, well-defined user stories and acceptance criteria
  • Prioritize backlog items based on risk, regulatory impact, value, and delivery timelines
  • Ensure traceability between user needs, system/software requirements, implementation, and verification activities

Scrum Master & Agile Execution

  • Serve as Scrum Master for one or more multi-disciplinary development teams
  • Facilitate agile ceremonies: backlog grooming, sprint planning, standups, sprint reviews, and retrospectives
  • Remove impediments and proactively manage dependencies across teams
  • Coach teams on agile best practices within a regulated development environment

Program & Stakeholder Interface

  • Act as the primary liaison between the technical team and Program Manager
  • Ensure development work aligns with program schedules, deliverables, and risk management plans
  • Communicate progress, risks, and tradeoffs clearly to program leadership and stakeholders
  • Support cross-functional coordination with Quality, Regulatory Affairs, Clinical, and Cybersecurity teams

Regulatory & Quality Alignment

  • Ensure agile artifacts support design controls, including documentation, traceability, and verification planning
  • Work within ISO 13485, IEC 62304, IEC 62366, and FDA design control requirements
  • Partner with Quality and Regulatory teams to ensure backlog items and increments are audit-ready
  • Support cybersecurity, safety, and risk management activities as part of product development

Requirements

Required Qualifications

  • Bachelor's Degree and 5+ years industry experience, with 2+ years in product ownership, scrum mastery, or technical program delivery
  • Hybrid environment but must be flexible and willing to work onsite for a minimum of 3 days per week
  • Experience working in medical device or other regulated product development environments
  • Strong understanding of Agile/Scrum frameworks and practical application in regulated settings
  • Ability to translate complex technical and regulatory requirements into actionable development work
  • Excellent communication skills across technical, quality, and executive stakeholders
  • Experience with development of software, firmware, or connected medical devices

Preferred Qualifications

  • Familiarity with FDA submissions (510(k), De Novo, PMA) and design history files (DHF)
  • Knowledge of cybersecurity for medical devices and secure product development
  • Experience working closely with Program Managers on multi-disciplinary development programs
  • Certified Scrum Master (CSM), SAFe, or Product Owner certification

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