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Medical Device Program Manager Jobs in Vermont (NOW HIRING)

Nolato AB

Quality Assurance Technician

Bethel, VT · On-site

... and management. Qualifications: * To succeed in this role, you must be obsessed with getting ... Two years of work history in Quality or Manufacturing is helpful - especially in the medical device ...

MedElite Group, LLC.

Travel Medical Assistant

Burlington, VT

$17.75 - $22.75/hr

Our partnership with MedElite Healthcare Management Group empowers us to focus on what matters most ... You will be assisting providers in Nursing Homes with a tablet device. A strong candidate will have ...

Akima, LLC

Site Lead

Williston, VT · On-site

The Site Lead supports the Program Manager in overseeing contractor personnel and managing site ... medical, dental, vision, life insurance, 401(k) and a range of other voluntary benefits. Paid Time ...

ZOLL Medical

Patient Service Representative

Burlington, VT · On-site

$17.50 - $22.25/hr

... Medical Corporation develops products to protect and manage cardiac patients, including the ... Program LifeVest ® according to the prescribing physician's orders * Measure the patient and ...

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All JobsMedical Device Program JobsMedical Device Program Manager JobsMedical Device Program Manager Jobs in Vermont

Medical Device Program Manager information

See Vermont salary details

$40.9K

$114.3K

$166.9K

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

As of Aug 6, 2026, the average yearly pay for medical device program manager in Vermont is $114,258.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,500.00 and $140,900.00 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 Vermont? For Medical Device Program Manager jobs in Vermont, the most frequently searched job titles are:
What job categories do people searching Medical Device Program Manager jobs in Vermont look for? The top searched job categories for Medical Device Program Manager jobs in Vermont are:
What cities in Vermont are hiring for Medical Device Program Manager jobs? Cities in Vermont 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 Vermont as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $114,258 per year, or $54.9 per hour.

Quality Assurance Technician

Nolato AB

Bethel, VT • On-site

Full-time

Re-posted 13 days ago

Job description

Nolato Vermont is looking for detailed oriented people to join us as Quality Assurance Technicians to help make sure we send only good product to our Customers!
Apply now
  1. Nolato Group
  2. Careers
  3. Open positions
  4. Nolato Vermont
  5. Quality Assurance Technician

Nolato is a global leader in precision injection molding and contract manufacturing for the world's most successful healthcare, automotive, and industrial OEMs.
Join an organization that is respected throughout the industry for our advanced technology, quality, and innovation - all while enjoying the benefits of stable ownership, a collaborative culture, professional development, continuing education, global opportunities, and an exceptional benefits package.
As a Quality Assurance Technician:
  • You'll work in either Bethel or Royalton, VT at our clean, climate-controlled production facilities - floor, office, lab - on a rotating 12-hour, 3/4 day per week schedule.
  • Reporting to the Quality Assurance Supervisor you'll make sure every product we produce meets our high standards and others like ISO 13485.
  • From collecting samples to inspecting product using measuring tools like micrometers, calipers, and vision systems - that's you.
  • You'll also make sure that all GMP and GDP tasks have been performed and are correct.
  • When needed, you'll be relied on to investigate quality issues and help solve production problems with your teammates and management.

Qualifications:
  • To succeed in this role, you must be obsessed with getting details right, have a mechanical aptitude, and have a High School diploma or GED equivalent.
  • Two years of work history in Quality or Manufacturing is helpful - especially in the medical device world or as an internal auditor - but not required.
  • We're the (quality) police of the company. You must be able to confidently and collaboratively address and solve problems with a variety of people.
  • You must care about doing the little things right, showing up on time, and being a helpful and respectful teammate.
  • You must be able to independently read and interpret documents such as safety rules, written instructions, operating, and quality procedures.
  • You should be able to accurately create detailed reports and records for management.
  • You must be able to stand for long periods of time and lift and carry up to 50 lbs.

Apply