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Medical Device Program Manager Jobs in Stuart, FL

Project Manager, R&D

Palm Beach Gardens, FL ยท On-site

$120K - $165K/yr

As a Program Manager within our Connected Care R&D organization , your contributions directly ... Oversee the endtoend lifecycle of a software medical device product from discovery through ...

Equipment Operator

Port Saint Lucie, FL ยท On-site

$16.50 - $22.50/hr

OCULUS is a family-owned medical device company founded and headquartered in Germany over 125 years ... Participate in training programs and continuous improvement initiatives * Support compliance with ...

Equipment Operator

Port Saint Lucie, FL ยท On-site

$16.50 - $22.50/hr

OCULUS is a family-owned medical device company founded and headquartered in Germany over 125 years ... Participate in training programs and continuous improvement initiatives * Support compliance with ...

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Showing results 1-20

Medical Device Program Manager information

See Stuart, FL salary details

$34K

$94.9K

$138.6K

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 Stuart, FL is $94,856.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,200.00 and $117,000.00 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 Stuart, FL? For Medical Device Program Manager jobs in Stuart, FL, the most frequently searched job titles are:
What job categories do people searching Medical Device Program Manager jobs in Stuart, FL look for? The top searched job categories for Medical Device Program Manager jobs in Stuart, FL are:
What cities near Stuart, FL are hiring for Medical Device Program Manager jobs? Cities near Stuart, FL with the most Medical Device Program Manager job openings:
Infographic showing various Medical Device Program Manager job openings in Stuart, FL 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 $94,856 per year, or $45.6 per hour.

Project Manager, R&D

Baxter

Palm Beach Gardens, FL โ€ข On-site

$120K - $165K/yr

Full-time

Medical, Dental, Life, Retirement, PTO

Re-posted 24 days ago


Job description

This is whereyour work makes a difference.

At Baxter, we believe every person-regardless of who they are or where they are from-deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job-you will find purpose and pride.

Your Role at Baxter

This is where your work saves lives.

The studies we undertake and the products we generate boost results for patients worldwide. As a Program Manager within our Connected Care R&D organization, your contributions directly influence patient outcomes and the reliability of the software-enabled medical devices clinicians depend on every day. It's demanding work - and you won't be doing it alone. Our teams collaborate across functions, lead through inspiration, and hold each other accountable.

Whether guiding a crossfunctional software team through a complex development cycle or coordinating with engineering, quality, and regulatory partners, you will help drive the delivery of Baxter's next-generation software medical device platform. Our R&D colleagues are motivated by meaningful impact, energized by teamwork, and skilled at influencing others to achieve outcomes.

What You'll Be Doing
  • Provide business and technical leadership for one or more software-focused R&D projects within Connected Care.

  • Lead teams in defining project strategies, establishing goals, and ensuring project scope is clearly defined and controlled.

  • Oversee the endtoend lifecycle of a software medical device product from discovery through requirements, development, verification, launch, and sustaining.

  • Engage regularly with all levels of management to ensure clear communication across teams and collaborators.

  • Guarantee identification and communication of project risks; develop mitigation plans and guide teams in proactive risk management.

  • Foresee potential conflict scenarios and drive resolutions that support mutually beneficial outcomes.

  • Drive continuous improvement initiatives across the software development lifecycle (SDLC).

  • Collaborate with other program managers to ensure successful launch of new products, including firsttime 510(k) submissions.

  • Hold teams accountable for execution, schedule adherence, and delivery of project commitments.

What You'll Bring
  • Bachelor's in Engineering (preferred) with 8+ years experience, or Master's with 5+ years.

  • 3+ years leading crossfunctional projects, ideally in software or regulated medical devices.

  • Strong command of SDLC, Quality Systems, and Agile project management.

  • Experience managing full product lifecycles - discovery through launch and sustaining.

  • Familiarity with FDA regulatory pathways (e.g., 510(k), combination products).

  • Proven ability to drive execution, manage scope, and proactively mitigate risks.

  • Excellent communication and presentation skills across technical and leadership audiences.

  • A selfstarter who thrives in fastmoving environments and challenges assumptions to drive decisions.

Baxter is committed to supporting the needs for flexibility in the workplace. We do so through our flexible workplace policy which includes a required minimum number of days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission. The flexible workplace policy is subject to local laws and legal requirements.At its discretion, Baxter may decide to adjust, suspend, or discontinue as business needs change.

We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $120,000-$165,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

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US Benefits at Baxter (except for Puerto Rico)

This is where your well-being matters. Baxter offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical and dental coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount, and the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees.For additional information regarding Baxter US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Baxter

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

Know Your Rights: Workplace Discrimination is Illegal

Reasonable Accommodations
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice
Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.