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Medical Device Product Development Engineer Jobs in Florida

Careerxchange

Product Development Engineer

Doral, FL

Product Development Engineer - Asia Manufacturing (Mandarin-Speaking) Location: Onsite or Hybrid (Travel Required) Job Summary We are looking for a hands-on Product Development Engineer with a strong ...

Raytheon

Product Development Engineer

Orlando, FL

CPR is seeking a Product Development Engineer (PDE) to join our team. The PDE section is ... Hired applicants may be eligible for benefits, including but not limited to, medical, dental ...

Raytheon

Product Development Engineer

Miami, FL

CPR is seeking a Product Development Engineer (PDE) to join our team. The PDE section is ... Hired applicants may be eligible for benefits, including but not limited to, medical, dental ...

Ford Motor Company

Product Development Engineer

Sunrise, FL · Hybrid

$68K - $114K/yr

Join the Ford Product Development team. Utilizing Design Thinking and User Experience methods, you ... Immediate medical, dental, vision and prescription drug coverage Flexible family care days, paid ...

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All JobsMedical Device Product Development Engineer JobsMedical Device Product Development Engineer Jobs in Florida

Medical Device Product Development Engineer information

See Florida salary details

$29.5K

$65.7K

$99K

How much do medical device product development engineer jobs pay per year?

As of Aug 17, 2026, the average yearly pay for medical device product development engineer in Florida is $65,675.00, according to ZipRecruiter salary data. Most workers in this role earn between $53,800.00 and $74,700.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a medical device product development engineer?

To thrive as a Medical Device Product Development Engineer, you need a strong background in biomedical, mechanical, or electrical engineering, along with knowledge of FDA regulations and product development processes. Familiarity with CAD software, prototyping tools, risk management systems, and regulatory standards such as ISO 13485 is typically required. Creativity, problem-solving, and effective teamwork are essential soft skills that drive innovation and ensure project success. These skills and qualifications are crucial for developing safe, effective medical devices that meet strict regulatory requirements and address real-world healthcare needs.

What are some common challenges medical device product development engineers face when working on new product designs?

Medical Device Product Development Engineers often navigate strict regulatory requirements and rigorous testing protocols to ensure product safety and compliance. Balancing innovative design with manufacturability and cost constraints can be challenging, as can coordinating input from cross-functional teams such as clinical, regulatory, and manufacturing. Additionally, managing project timelines while accommodating iterative design changes based on feedback or testing results requires strong organizational and communication skills.

What does a medical device product development engineer do?

A Medical Device Product Development Engineer is responsible for designing, developing, and testing medical devices to ensure they are safe, effective, and compliant with regulatory standards. They work closely with cross-functional teams, including quality assurance, regulatory affairs, and manufacturing, to take products from concept through to production. Their tasks often include prototyping, risk assessment, documentation, and troubleshooting any issues that arise during the development process. Additionally, they must stay updated on industry standards and regulations to ensure that products meet all necessary requirements for market approval.

What is the difference between Medical Device Product Development Engineer vs Quality Assurance Engineer?

AspectMedical Device Product Development EngineerQuality Assurance Engineer
CredentialsEngineering degree, certifications like PMP or Six Sigma often preferredEngineering or science degree, certifications like CQE or ISO auditor training
Work EnvironmentDesign labs, R&D departments, cross-functional teamsManufacturing facilities, quality control labs, compliance departments
Industry UsageInvolved in designing and developing new medical devicesEnsures products meet quality standards and regulatory requirements

While both roles are essential in the medical device industry, the Medical Device Product Development Engineer focuses on creating and improving devices, whereas the Quality Assurance Engineer ensures these devices meet safety and quality standards. Understanding these differences helps in choosing the right career path or job search focus.

What are popular job titles related to Medical Device Product Development Engineer jobs in Florida?

For Medical Device Product Development Engineer jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Medical Device Product Development Engineer jobs in Florida look for?

The top searched job categories for Medical Device Product Development Engineer jobs in Florida are:

What cities in Florida are hiring for Medical Device Product Development Engineer jobs?

Cities in Florida with the most Medical Device Product Development Engineer job openings:

Medical Device Product Development Engineer jobs near you
Infographic showing various Medical Device Product Development Engineer job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $65,675 per year, or $31.6 per hour.

Product Development Manager - Medical Device

International Medical Industries

Pompano Beach, FL • On-site

$107K - $134K/yr

Full-time

Posted 18 days ago

Job description

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

Requirements

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 an uninstructed 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.

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