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Medical Device Development Jobs in Florida (NOW HIRING)

Arthrex

Manager - Organizational Development

Naples, FL · On-site

Manager - Organizational Development Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex Human Resources department ...

ARTHREX

Manager - Organizational Development

Naples, FL · On-site

Manager - Organizational Development Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex Human Resources department ...

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Showing results 41-60

All JobsMedical Device Development JobsMedical Device Development Jobs in Florida

Medical Device Development information

See Florida salary details

$21.7K

$39.9K

$60.5K

How much do medical device development jobs pay per year?

As of Sep 4, 2026, the average yearly pay for medical device development in Florida is $39,919.00, according to ZipRecruiter salary data. Most workers in this role earn between $31,800.00 and $44,800.00 per year, depending on experience, location, and employer.

What is medical device development?

Medical device development is the process of designing, creating, testing, and bringing medical devices to market. This process involves multiple stages, including concept development, prototyping, preclinical and clinical testing, regulatory approval, and manufacturing. The goal is to ensure that new devices are safe, effective, and meet regulatory standards before they are used by healthcare professionals or patients. Teams in medical device development often include engineers, scientists, regulatory specialists, and quality assurance professionals.

What are the key skills and qualifications needed to thrive in medical device development, and why are they important?

To thrive in Medical Device Development, you need expertise in engineering or life sciences, a solid understanding of regulatory requirements, and often an advanced degree such as a master's or Ph.D. in a relevant field. Familiarity with CAD software, prototyping tools, and knowledge of FDA or ISO regulatory standards is typically required. Strong problem-solving abilities, collaboration, and effective communication distinguish top professionals in this field. These skills ensure the development of safe, innovative, and compliant medical devices that meet both user needs and regulatory standards.

What are some common challenges faced by professionals in medical device development, and how can they be addressed?

Professionals in medical device development frequently encounter challenges such as navigating complex regulatory requirements, ensuring product safety and efficacy, and managing cross-functional collaboration between engineering, clinical, and regulatory teams. Addressing these challenges requires staying updated on evolving regulations, fostering open communication among diverse team members, and implementing robust quality control processes. Proactively engaging with regulatory bodies and regularly reviewing project milestones can help streamline development and reduce the risk of costly delays.

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

AspectMedical Device DevelopmentMedical Device Quality Assurance
CredentialsEngineering degrees, certifications like RAPS or regulatory trainingQuality certifications, ISO 13485, regulatory compliance training
Work EnvironmentDesign labs, R&D teams, product development settingsManufacturing sites, quality control labs, compliance departments
Industry UsageDesigning and creating new medical devicesEnsuring devices meet quality and regulatory standards

Medical Device Development focuses on designing and creating new medical devices, involving engineering and product innovation. Medical Device Quality Assurance ensures these devices meet safety, quality, and regulatory standards through testing and compliance processes. Both roles are essential in the medical device industry but serve different functions in the product lifecycle.

Medical Device Development jobs near you
Infographic showing various Medical Device Development job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, and 5% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $39,919 per year, or $19.2 per hour.

Principal Research & Development (R&D) Engineer

Treace

Ponte Vedra, FL • On-site

Full-time

Re-posted 23 days ago

Job description

Company Description

Treace's mission is to be the leader in the surgical treatment of bunions by establishing the Lapiplasty System as the standard of care. We are committed to operating our business with the highest standards of ethical conduct. We intend to exceed our customers' expectations through an innovation-driven, high-velocity approach to solving treatment and surgical problems. With our products and services, our mission is to assist foot and ankle surgeons in improving patient outcomes and reducing healthcare costs, while providing rewarding experiences and opportunities for our employees and stakeholders.

Job Description

Are you a technical expert and innovative leader looking to make a significant impact in product design and development? We are seeking a Principal R&D Engineer to manage and execute key design projects while mentoring other engineers. This role offers the opportunity to lead major product development initiatives from concept to production and contribute to the company's short-term and long-term goals.

Primary Duties & Responsibilities

As a Principal R&D Engineer, your responsibilities include:

  • Leading, participating in, and supporting activities throughout product development, including:
    • Concept generation
    • Project planning, design, and execution stages
    • Prototyping, design for manufacturability (DFM), design for inspection (DFI)
    • Risk assessments, pilot production, and design reviews
    • Verification, validation, and testing (protocol authorship, physical testing, reports)
    • Pre-production and full production launch
  • Demonstrating expertise in material selection, manufacturing methods, inspection techniques, and critical measurements.
  • Engaging directly with customers alongside sales and marketing to gather design ideas, document concepts, and transition them into high-quality production-ready products.
  • Ensuring compliance with the company's design quality system.

We're looking for candidates with the following qualifications:

Design Expertise - Expert CAD knowledge (preferably SolidWorks) for creating parametric models and ASME Y14.5-compliant prints.

Manufacturing Feasibility - Proficient in interacting with design and manufacturing teams to balance manufacturability, reliability, and cost-effectiveness.

Analytical and Technical Expertise - Advanced knowledge of CAD design, 3D print generation, FEA simulations, and ISO standards.

Communication and Leadership - Strong ability to communicate schedules, budgets, designs, and testing results effectively to teams and stakeholders.

Customer-Centric Approach - Ability to generate product designs based on customer input and surgeon feedback.

Hands-On Approach - Comfort with cadaver work, surgical settings, and detailed research experiments to test feasibility.

Collaborative Team Player - Proven ability to work on cross-functional teams and assist in creating design documentation for medical devices.

To excel in this role, you should demonstrate:

  • Exceptional organizational and communication skills.
  • Strong attention to detail.
  • Expertise in product development, material selection, and industry best practices.
  • A desire to work on complex engineering problems and mentor your peers to grow the team's capabilities.

Educational and Software Proficiency

  • Advanced experience using Microsoft Office tools (Word, Excel, PowerPoint, Project).
  • SolidWorks proficiency required; familiarity with FEA and GD&T is a must.
Qualifications
  • Bachelor's degree in Mechanical Engineering or equivalent engineering discipline
  • 7+ years' mechanical design and manufacturing experience of which 5+ years of actual product development experience bringing innovative product to market from conception to launch in  regulated industry. (Preference is given to medical device development).
Additional Information

All your information will be kept confidential according to EEO guidelines.

Treace's Privacy Policy

It is Treace's policy not to discriminate against any applicant for employment, or any employee because of age, color, sex, disability, national origin, race, religion, veteran status or any other characteristic protected by applicable law. EEO/Disabled/Veterans Employer
 

Treace is a drug free employer.

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