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Medical Device Development Jobs in Florida (NOW HIRING)

Advanced Medical Supply

Medical Device Sales Rep

Tampa, FL · On-site

$84K - $114K/yr

We are a diverse and fast growing medical device & equipment company that is committed to focusing ... Understand and execute sales territory management and customer development. * Establish and ...

Advanced Medical Supply

Medical Device Sales Rep

Tampa, FL · On-site

$84K - $114K/yr

We are a diverse and fast growing medical device & equipment company that is committed to focusing ... Understand and execute sales territory management and customer development. * Establish and ...

Crown Medical, Inc.

Medical Territory Device Rep

Naples, FL · On-site

$90K - $120K/yr

We are a fully integrated company with internal resources dedicated to the development and promotion of medical supplies and device products. We believe that our proven products and customer focused ...

Crown Medical, Inc.

Medical Territory Device Rep

Miami, FL · On-site

$90K - $120K/yr

We are a fully integrated company with internal resources dedicated to the development and promotion of medical supplies and device products. We believe that our proven products and customer focused ...

Endo-Therapeutics, Inc.

Be Seen First

Product Development Engineer III

Clearwater, FL · On-site

$84K - $104K/yr

Knowledge of plastic injection mold design and process EDUCATION/ TRAINING: * BS/MS in Mechanical, Biomedical, or Electrico-Mechanical Engineering. * 7+ years in medical device development ...

HIRE-IQ

Sales Manager - Medical Device

Orlando, FL

$75K - $100K/yr

HIRE-IQ is recruiting a full-time Sales Manager for a well-established medical device company. The ... Collaborate closely with marketing, customer service, and commercial development teams to drive ...

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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 Jun 6, 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 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 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.

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 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 popular job titles related to Medical Device Development jobs in Florida? For Medical Device Development jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Medical Device Development jobs in Florida look for? The top searched job categories for Medical Device Development jobs in Florida are:
Medical Device Development jobs near you
Infographic showing various Medical Device Development job openings in Florida as of May 2026, with employment types broken down into 89% Full Time, 2% Part Time, and 9% Contract. Highlights an 94% In-person, 4% Hybrid, and 2% Remote job distribution, with an average salary of $39,919 per year, or $19.2 per hour.

Electrical HW Test Engineer with Medical Device

Kaav Inc.

Orlando, FL • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Hiring For Electrical HW Test Engineer with Medical Device
C2C, Full Time
Location: Philips Orlando FL ( Onsite )
Exp:6+
Responsibilities
The
Electrical HW Test
Engineer
will be a member of the Product Development staff and be
involved in the design, development, and maintenance of new MRI compatible products.
•Able to analyze and debug mixed signal PCA in embedded battery operating systems.
•Familiar with low-level analog front-end signal measurement, including amplifiers, filters,
sensors, and ADC, using an oscilloscope with a single probe and/or differential probe.
•Able to perform signal integrity tests on common high-speed digital interfaces (e.g. I2C, SPI,
UART, QSPI, USB, SWD, etc) using a logic analyzer.
•Able to deep dive into the schematics, datasheet, and layout for debugging and
troubleshooting.
•Able to perform power estimation and thermal analysis on a board level.
•Able to perform system-level integration testing including mechanical model, battery, cables,
sensor, charger, etc.
•Experience with various medical industry regulatory testing, including ESD, EMI, EFT, etc.
•Experience with BLE device testing and familiarity with spectrum and network analyzers.
•Able to effectively collaborate with the cross-functional team to perform system-level tests and
evaluations.
•Proficient in documenting test procedures, results, and issues.
•Able to travel to the Clevland MR site to conduct MR-related testing.
Desirable
•Class 2 or Class 3 medical device development experience.
•Understanding of global regulatory requirements for medical devices.
•LEAN/Six Sigma certification or experience.
•Experience in the field of Medical Devices product design e.g. CT, MR, X-Ray,
Mammography systems etc. will be an added advantage
•Exposure to International Medical Quality and Regulatory Standards e.g. IEC, FDA, UL, CE
is a plus
Interested Candidates Can Send their resume to mahesh.b@kaavinc.com
Thanks & Regards,
B. Mahesh
Sr. US IT Recruiter
Kaav Inc.3925 75th St, Suite 101 A, Aurora, IL - 60504
Email: mahesh.b@kaavinc.com :: P: 847-450-7769
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