ZipRecruiter

Log In

1

Medical Device Program Manager Jobs in Bristol, RI

Integrated Resources INC

Medical Writer

Raynham, MA · On-site

Medical Writing Specialist Division: Strategic Medical Affairs Reports To: Medical Safety Project ... device/drug development processes, regulatory requirements, good clinical and data management ...

GDR Defense

Production Manager - Mansfield, MA

Mansfield, MA · On-site

$100K - $120K/yr

Direct process improvement programs and manufacturing process excellence. * Lead teams in achieving ... Demonstrated medical device production management experience required. * Experience with Class III ...

next page

Showing results 1-20

All JobsMedical Device Program JobsMedical Device Program Manager JobsMedical Device Program Manager Jobs in Bristol, RI

Medical Device Program Manager information

See Bristol, RI salary details

$40.2K

$112.2K

$163.9K

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 Bristol, RI is $112,200.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,000.00 and $138,300.00 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 job categories do people searching Medical Device Program Manager jobs in Bristol, RI look for?

The top searched job categories for Medical Device Program Manager jobs in Bristol, RI are:

What cities near Bristol, RI are hiring for Medical Device Program Manager jobs?

Cities near Bristol, RI 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 Bristol, RI as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 19% Part Time, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $112,200 per year, or $53.9 per hour.

Regulatory Affairs Program Manager

Stark Pharma Solutions Inc

Raynham, MA • On-site

Contractor

Re-posted 20 days ago

Job description

Hi,

My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Regulatory Affairs Program Manager position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows

Job Title: Regulatory Affairs Program Manager (Medical Device – Divestiture)

Location: Raynham, MA / West Chester, PA / Palm Beach Gardens, FL (Hybrid – 3–4 days onsite)
Duration: 12+ Months (Extension Possible)
 

We are seeking an experienced Regulatory Affairs Program Manager to lead a large-scale Medical Device Divestiture initiative. This role will manage the transfer of global regulatory registrations, submissions, and documentation from a large healthcare organization to a newly established medical device company while ensuring regulatory compliance and seamless execution.

Key Responsibilities:

  • Lead regulatory activities supporting a global divestiture program.
  • Complete and execute the Regulatory Registration Transfer Strategy.
  • Manage ownership transfers, amendments, renewals, notifications, and new submissions.
  • Coordinate with cross-functional Regulatory, Quality, and Project teams.
  • Identify project risks, develop mitigation plans, and ensure GMP compliance.
  • Maintain project documentation, timelines, and stakeholder communication.

Required Skills:

  • 10+ years of Regulatory Affairs experience in the Medical Device industry.
  • Hands-on experience with Divestiture/Business Separation projects.
  • Strong Regulatory Program Management experience.
  • Expertise with FDA 510(k), PMA, global registrations, labeling changes, design changes, and regulatory submissions.
  • Knowledge of registration ownership transfers, submission pathways, and health authority interactions.
  • Excellent communication, leadership, and stakeholder management skills.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/

Thank you,

Karthik Mutyala

Recruiting Manager

Stark Pharma Solutions Inc

Email: karthik@starkpharma.com

15 Corporate Place S, Suite 350,

Piscataway, New Jersey 08854

www.starkpharma.com