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Product Manager Medical Device Jobs in Boca Raton, FL

Medical Device Manufacturing Co

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Product Development Manager - Medical Device

Pompano Beach, FL · On-site

$107K - $134K/yr

... the medical device industry. * 3+ years in a leadership role within product development ... Change management: willing to make hard fact-based decisions, comfortable with anuninstructed and ...

New

Crown Medical, Inc.

Medical Device Rep

Boca Raton, FL · On-site

$82K - $113K/yr

Medical Sales Territory Representative - Entry Level We are a leading Medical Device and Equipment ... product knowledge by completing required training courses, working with your managers, and ...

Medical Device Distribution Company

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Product Quality Inspection Specialist

Miami Gardens, FL · On-site

$70K - $80K/yr

Participate in change management, internal audits, supplier quality initiatives, and continuous ... Minimum 3-5 years of professional quality experience within medical device, veterinary product ...

Medical Device Distribution Company

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Product Quality Inspection Specialist

Miami Gardens, FL · On-site

$70K - $80K/yr

Participate in change management, internal audits, supplier quality initiatives, and continuous ... Minimum 3-5 years of professional quality experience within medical device, veterinary product ...

Crown Medical, Inc.

Medical Orthopedic Rep

Hollywood, FL · On-site

$91K - $122K/yr

... device products. We believe that our proven products and customer focused marketing and sales ... Ability to effectively manage a physician-based customer base * Skills to communicate clinically ...

Lund Boats

Product Manager

Pompano Beach, FL · On-site

$115K - $130K/yr

We are seeking a Product Manager to develop and execute product line strategy for the Sea Choice ... including medical, dental, vision, paid vacation, 401k (up to 4% match), Health Savings Account ...

Open Scientific

Regulatory Manager

Sunrise, FL · On-site

Develop medical device regulatory submissions in accordance with FDA requirements (e.g., pre ... products. Partner with cross functional teams by providing independent regulatory guidance and ...

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Product Manager Medical Device information

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$66

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How much do product manager medical device jobs pay per hour?

As of Aug 1, 2026, the average hourly pay for product manager medical device in Boca Raton, FL is $66.15, according to ZipRecruiter salary data. Most workers in this role earn between $62.74 and $69.57 per hour, depending on experience, location, and employer.

What are some common challenges faced by Product Managers in the medical device industry, and how can they be addressed?

Product Managers in the medical device field often navigate strict regulatory requirements, complex cross-functional collaboration, and the need to balance innovation with patient safety. Staying current with evolving FDA and international regulations is essential, as is fostering clear communication between engineering, clinical, and marketing teams. Building strong relationships with stakeholders and having a structured process for gathering user feedback can help address these challenges and ensure the product meets clinical needs and compliance standards.

What Is the Job of a Medical Device Product Manager?

The job duties of a medical device product manager may include managing the technical aspects of product design and development, and defining the target market that the product serves. Your responsibilities in this role may consist of planning the process that the company uses to develop a medical device. This process may include obtaining relevant documentation and approval from medical regulatory bodies. Some medical device product managers focus on marketing products by developing a marketing strategy, defining a target market, and coming up with a pricing strategy.

What does a Product Manager do in the medical device industry?

A Product Manager in the medical device industry oversees the development and lifecycle of medical products, from concept through launch and post-market support. They collaborate with cross-functional teams such as engineering, regulatory, marketing, and sales to ensure products meet both customer needs and regulatory requirements. Their responsibilities may include market research, defining product requirements, managing timelines, and creating go-to-market strategies. The goal is to deliver safe, effective, and competitive medical devices that improve patient outcomes.

What are the key skills and qualifications needed to thrive as a Product Manager in Medical Devices, and why are they important?

To thrive as a Product Manager in Medical Devices, you need a background in engineering, life sciences, or business, combined with knowledge of product development and regulatory requirements. Familiarity with tools like project management software, CRM systems, and understanding of FDA or CE Mark processes is typically required. Strong communication, problem-solving, and stakeholder management skills set outstanding candidates apart in this field. These skills ensure safe, compliant, and market-driven product launches that meet both user needs and regulatory standards.

What is the difference between Product Manager Medical Device vs Regulatory Affairs Specialist in the medical device industry?

AspectProduct Manager Medical DeviceRegulatory Affairs Specialist
Required CredentialsBachelor's degree, experience in product management, knowledge of medical devicesBachelor's degree, certification in regulatory affairs, knowledge of FDA regulations
Work EnvironmentCross-functional teams, product development, marketingRegulatory compliance, documentation, liaising with authorities
Employer & Industry UsageMedical device companies, healthcare firmsMedical device manufacturers, regulatory agencies
Common Search & Comparison IntentUnderstanding roles in product developmentUnderstanding regulatory responsibilities

The Product Manager Medical Device focuses on developing, launching, and managing medical device products, ensuring market success. In contrast, the Regulatory Affairs Specialist ensures products meet regulatory standards and obtain necessary approvals. Both roles are essential in the medical device industry but serve different functions within the product lifecycle.

More about Product Manager Medical Device jobs
What are popular job titles related to Product Manager Medical Device jobs in Boca Raton, FL? For Product Manager Medical Device jobs in Boca Raton, FL, the most frequently searched job titles are:
What job categories do people searching Product Manager Medical Device jobs in Boca Raton, FL look for? The top searched job categories for Product Manager Medical Device jobs in Boca Raton, FL are:
What cities near Boca Raton, FL are hiring for Product Manager Medical Device jobs? Cities near Boca Raton, FL with the most Product Manager Medical Device job openings:
Product Manager Medical Device jobs near you
Infographic showing various Product Manager Medical Device job openings in Boca Raton, FL as of July 2026, with employment types broken down into 77% Full Time, 15% Part Time, and 8% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $137,600 per year, or $66.2 per hour.

Product Development Manager - Medical Device

Medical Device Manufacturing Co

Pompano Beach, FL • On-site

$107K - $134K/yr

Full-time

Medical, Dental, Vision, Life, PTO

Posted 2 days ago

New

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Job description

Departmental Manager providing direct management of engineers, supervisors, and technicians. Allocates resources based upon departmental plans & budgets. Responsible for hire/fire decisions within their department. Submits departmental budgets, performance / productivity targets and reports on results. Measured against performance plan goals and objectives.


The primary role of the Product Development Manager is to plan, organize and direct engineers to meet company objectives for design, development of new products and make improvements to existing products by performing the following duties personally or through subordinates. This manager ensures that all engineering activities are completed on time and conform to the standards as established by design control procedures.


Duties and Responsibilities:

• Supervise the team of engineers within the product development department.

• Responsible for the development of new products as determined by the company’s product development roadmap. Continually researches for new methods or components to enhance or improve existing products.

• Prepare and/or review engineering change requests; coordinate cross functional teams to determine feasibility, develop and oversee preparation and implementation of all engineering change notices and document change control.

• Responsible for maintaining and implementing processes and procedures covered by design control.

• Assist quality and compliance in the implementation of the quality system including but not limited to support in conducting risk analysis, closing customer complaints, CARs, internal audits, and other activities covered by the quality system.

• Assist manufacturing operations with development of processes, tooling, molds, and design transfer necessary to produce new products.

• Provide customer service and sales & marketing departments with orientation and training on new products, and assist with preparation of sales presentations, service/repair methods, and marketing literature.

• Perform other duties as assigned.


Required Qualifications:

• Bachelor’s degree in mechanical engineering.

• Minimum 5+ years of engineering experience within the medical device industry.

• 3+ years in a leadership role within product development, engineering, design, etc.

• Experience with GMP and other regulatory compliance requirements.

• Experience with design & development of medical devices within a design control process.

• Prior hands-on customer interaction and proven experience understanding the voice of the customer.

• Change management: willing to make hard fact-based decisions, comfortable with anuninstructed and changing environment.

• Skilled at developing new ideas from both a product and process perspective.

• Demonstrated practical application of design FMEA, value engineering, and design for manufacturability concepts.

• Extensive experience in 3D CAD modeling and 2D dimensioning using Solidworks.


Physical / Mental Demands:

• Working conditions are normal for an office environment.

• Work may require weekend and evening work.

• Work may require travel.

• Physical activity includes sitting, walking, standing, bending, squatting, reaching above shoulders and lifting up to 40 pounds.

• Work under stress in a fast-paced environment.

• Must be alert, able to concentrate, and use good judgment.


Company Description

IMI specializes in tamper-evident technologies that help prevent drug diversion and misuse. Our solutions are essential to hospital and pharmacy drug security programs.