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Medical Device Program Manager Jobs in Rhode Island

Veranex

Senior Program Manager

Minneapolis, MN · On-site

$145K - $208K/yr

About This Role The Senior Program Manager is a senior leadership role responsible for driving the ... Lead cross-functional medical device development programs as Core Team Leader * Establish team ...

Cadence Inc

Supply Chain Manager

Cranston, RI · On-site

... 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 ...

Innovative Construction

Program Manager

Tiverton, RI · On-site

$100/hr

Job: Project Manager Location: Tiverton, RI Join Innovative Construction, Inc. Innovative ... Medical, dental, and vision insurance * 401(k) with company benefits * Paid vacation * Continuing ...

New

Innovative Construction

Program Manager

Tiverton, RI · On-site

$100/hr

Job: Project Manager Location: Tiverton, RI Join Innovative Construction, Inc. Innovative ... Medical, dental, and vision insurance * 401(k) with company benefits * Paid vacation * Continuing ...

NWN Carousel

Program Manager (Southwest)

Exeter, RI · On-site +1

Responsibilities The NWN Program Manager is responsible for managing complex programs and leading a ... This includes medical, dental, and vision plans, Health Savings Account (HSA) and Flexible Spending ...

Zimmer, Inc.

Senior Quality Manager

Providence, RI · On-site

$130K - $160K/yr

What You Can Expect This is an onsite role at our site in Norfolk, Virginia Site Quality leader and Management Representative responsible for directing the quality function a medical device design ...

Zimmer, Inc.

Senior Quality Manager

Providence, RI · On-site

$130K - $160K/yr

What You Can Expect This is an onsite role at our site in Norfolk, Virginia Site Quality leader and Management Representative responsible for directing the quality function a medical device design ...

NinjaOne

Vulnerability & Cloud Security Program Manager

NC · On-site +1

$180K - $220K/yr

... and mobile device management. What You'll Love  We are a collaborative, kind, and curious ... We have you covered with our comprehensive benefits package, which includes medical, dental, and ...

Veranex

Sr Mechanical Engineer

Providence, RI · On-site

$93K - $121K/yr

Thorough knowledge of product development and strong understanding of the medical device industry ... Strong ability to manage multiple tasks and projects effectively. * Familiarity with FDA, QSR, and ...

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Showing results 1-20

All JobsMedical Device Program JobsMedical Device Program Manager JobsMedical Device Program Manager Jobs in Rhode Island

Medical Device Program Manager information

See Rhode Island salary details

$37.7K

$105.2K

$153.8K

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 Rhode Island is $105,237.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,900.00 and $129,800.00 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 Rhode Island? For Medical Device Program Manager jobs in Rhode Island, the most frequently searched job titles are:
What job categories do people searching Medical Device Program Manager jobs in Rhode Island look for? The top searched job categories for Medical Device Program Manager jobs in Rhode Island are:
What cities in Rhode Island are hiring for Medical Device Program Manager jobs? Cities in Rhode Island 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 Rhode Island as of July 2026, with employment types broken down into 72% Full Time, 21% Part Time, and 7% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $105,237 per year, or $50.6 per hour.
Senior Program Manager

Senior Program Manager

Veranex

Minneapolis, MN • On-site

$145K - $208K/yr

Full-time

Re-posted 13 days ago

Job description

Veranex's mission as an Innovation CRO is to improve patient outcomes by accelerating our clients' innovations to market. As the world's only end-to-end professional services firm focused on MedTech, we take clients' Vision to Velocity through our comprehensive service portfolio, with expertise in human centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting.
About This Role
The Senior Program Manager is a senior leadership role responsible for driving the successful execution of complex, cross-functional medical device development programs. Serving as a Core Team Leader, this individual is accountable for end-to-end program delivery, ensuring projects meet scope, schedule, budget, quality, and regulatory requirements.
This role combines program execution, technical leadership, client engagement, and business development support, guiding programs across the full product lifecycle-from concept through commercialization-while aligning internal teams and client expectations.
What You'll Do
  • Lead cross-functional medical device development programs as Core Team Leader
  • Establish team structure, roles, accountability, and governance alignment
  • Drive end-to-end program execution including scope, schedule, and budget management
  • Develop and maintain program plans, milestones, and deliverables
  • Monitor project performance using KPIs (schedule, budget, risk, deliverables)
  • Identify and mitigate business and technical risks proactively to ensure successful outcomes
  • Ensure compliance with design control processes and regulatory requirements
  • Act as primary point of contact for clients; lead program communications and reviews
  • Align program delivery with client goals, regulatory strategies, and commercialization timelines
  • Facilitate collaboration across engineering, regulatory, quality, clinical, and operations teams
  • Provide program updates and escalation reporting to PMO and executive stakeholders
  • Ensure adherence to PMO governance frameworks and best practices
  • Support continuous improvement and lessons learned initiatives
  • Support business development with project extensions and change orders
  • Travel as needed to support program and client needs

Qualifications
Required:
  • Bachelor's degree in Engineering, Biomedical Engineering, or a related technical field
  • 10+ years of experience in medical device development or program management
  • Demonstrated experience leading cross-functional product development programs
  • Strong knowledge of medical device design controls and full development lifecycle
  • Experience operating in FDA-regulated and ISO-certified environments
  • Expertise in program management methodologies (scope, schedule, cost, risk, stakeholders)
  • Strong financial acumen including budgeting, forecasting, and resource planning
  • Excellent communication, stakeholder management, and leadership skills
  • Ability to manage multiple priorities with minimal supervision
  • Experience with program management tools (e.g., MS Project, Smartsheet, Jira)
  • Willingness to travel as required
  • Hybrid work environment based in Providence, RI

Preferred:
  • Master's degree in Engineering or related discipline
  • PMP certification or equivalent
  • Experience in consulting or external product development environments
  • Understanding of regulatory pathways (e.g., 510(k), PMA, IDE, CE Mark)
  • Experience interpreting RFPs and developing executable program strategies

Veranex is an equal opportunity employer and prohibits discrimination of any kind. All qualified applicants will receive consideration for employment without regard for race, color, religion or belief, sex (including pregnancy, gender identity or gender expression), sexual orientation, parental or marital status, disability, age, status as a protected veteran, national, social, or ethnic origin, or any other applicable legally protected characteristics.

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