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Medical Device Program Manager Jobs in Rhode Island

Brownhealth

Outreach Program Manager

Pawtucket, RI

Assesses to determine program eligibility, engagement in treatment, appropriate level of care ... medical or clinical practitioners. Facilitates scheduling of appointments. * Provides daily ...

Lancesoft INC

Packaging Engineer II

Warwick, RI · On-site

$50 - $55/hr

Title: Packaging Engineer II Contract duration: 12+months Must Have * • Ability to manage ... Medical Device Design Control * Packaging Engineering * Protocols writing * Scientific Technical ...

Brownhealth

Biomedical Equip Tech II

Providence, RI · On-site

Works under general supervision of the Manager of Medical Engineering, performs a variety of tasks ... One to three years' experience working in a healthcare or medical device manufacture environment ...

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Showing results 21-40

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 28, 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 74% Full Time, 19% 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.
Process Development Engineer I

Process Development Engineer I

Confluent Medical Technologies

Warwick, RI • On-site

$59K - $98K/yr

Full-time

Posted 4 days ago

Job description

Salary Range:
$59,300.00 - $98,750.00
Job Description:
Process Engineer I - Laser
Confluent Medical Technologies has set the standard for medical-device
technology and innovation! We are a comprehensive partner with our customers,
offering complete materials, components, and design and development services.
Are you intellectually curious? Have you been working with lasers and
understand their intricate components? You may be just who we are looking for!
We are seeking a Process Engineer I - Laser reporting to Senior Manager, Engineering to join our dynamic team of industry leading experts at our Warwick, RI facility.
As a uniquely qualified candidate, you will:
• Responsible for process development - from proof-of-concept prototypes
to sustained manufacturing validation - planning, and coordinating
engineering activities, studies and programs in support of standard
production and new product development related to laser cutting.
• Hands on process development -ability to run lasers, cut parts and
troubleshoot systems.
• Experience translating customer drawings into laser cutting programs
using Solidworks and AutoCAD in accordance with GD&T principles.
• Ability to review and analyze data using statistical tools such as DOE's,
CPK/PPK, and ANOVA variation analysis.
• Create, communicate, and maintain documentation per quality control
policies.
• Production support.
• Expert in organizational skills about data gathering, organizing and basic
analysis.
• Possess good English communication skills - both written and oral.
• Follow health, safety and environmental programs for preventative
maintenance - adhering to safety protocols and ensuring that all hazards
are properly managed.
Requirements:
• Bachelor of engineering degree in the area of mechanical engineering or
comparable curriculum is required.
• Have solid background in CAD Software such as AutoCad, Solidworks
etc.
• Have 3D printing experience
• Have laser experience.
• Possess 1-3 years of experience in Micromachining or Optical Metrology.
• Have machine maintenance expertise.
• Experience in the medical device industry.
• Possess good English communication skills - both written and oral.
Confluent Medical Technologies is dedicated to working collaboratively with our customers, taking their projects from rapid prototype into high volume production. Our unparalleled technical expertise, proven experience and partnership with our clients has allowed us to perfect the process necessary to deliver world-class medical devices through innovative material science, engineering, and manufacturing. Our primary capabilities include: Nitinol components and tubing, balloon expandable stents and catheters, complex catheters, biomedical textiles, and high precision polymer tubing. We take pride in our position as the leader in the medical technology space and are driven by a passion to create products that our clients have envisioned for their customers.
We regret that we are unable to sponsor employment visas or consider individuals on time-limited visa status for this position.
Confluent Medical Technologies is an equal opportunity employer.
Only qualified candidates will be contacted.

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