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Intern Medical Device Engineer Jobs in Florida (NOW HIRING)

Cordis

Sr R&D Engineer (Onsite)

Miami Lakes, FL · On-site

$94K - $130K/yr

Applies comprehensive medical device engineering knowledge and a thorough understanding of concepts, principles, and technical capabilities to perform varied tasks and projects. * May contribute to ...

New

Cordis

Sr R&D Engineer (Onsite)

Miami Lakes, FL · On-site

$94K - $130K/yr

Applies comprehensive medical device engineering knowledge and a thorough understanding of concepts, principles, and technical capabilities to perform varied tasks and projects. * May contribute to ...

atrion

Quality Engineer

Davie, FL

$66K - $85K/yr

Manages engineering projects. Supports the internal and external audit program. Uses statistical ... A minimum of 5 years' experience in the medical device manufacturing industry is preferred.

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All JobsIntern Medical Device Engineer JobsIntern Medical Device Engineer Jobs in Florida

Intern Medical Device Engineer information

What does an intern medical device engineer do?

An Intern Medical Device Engineer assists in the design, development, and testing of medical devices under the supervision of experienced engineers. Their responsibilities may include conducting research, creating prototypes, analyzing data, and ensuring products meet regulatory standards. Interns often collaborate with cross-functional teams and gain hands-on experience in the medical device industry. This role provides valuable exposure to engineering processes and helps interns build skills required for a future career in biomedical engineering.

What types of projects and responsibilities can an intern medical device engineer expect during their internship?

As an Intern Medical Device Engineer, you can expect to participate in hands-on projects such as assisting in prototype development, performing laboratory testing, and collecting and analyzing data for product improvement. You'll often work closely with senior engineers, quality assurance teams, and regulatory specialists to ensure devices meet safety and compliance standards. Interns may also help prepare technical documentation and contribute to brainstorming sessions for new product features, providing a well-rounded exposure to the medical device development process. This collaborative environment offers valuable experience and networking opportunities for future career growth.

What are the key skills and qualifications needed to thrive as an intern medical device engineer?

To thrive as an Intern Medical Device Engineer, you need a solid background in biomedical engineering or a related field, along with foundational knowledge of device design and regulatory standards. Familiarity with CAD software, prototyping tools, and basic laboratory testing equipment is typically required, and coursework or certification in medical device regulations can be advantageous. Strong problem-solving, teamwork, and communication skills help interns contribute effectively to multidisciplinary projects and adapt to feedback. These competencies are crucial for ensuring safe, innovative device development and successful collaboration in a regulated industry.

What is the difference between Intern Medical Device Engineer vs Junior Medical Device Engineer?

AspectIntern Medical Device EngineerJunior Medical Device Engineer
CredentialsTypically pursuing or recently completed a relevant degreeBachelor's or Master's in biomedical, mechanical, or related engineering
Work EnvironmentInternship setting, supervised, learning-focusedEntry-level professional role, more independent tasks
Employer & Industry UsageMedical device companies, research labs, internshipsMedical device companies, manufacturing, R&D teams

Intern Medical Device Engineers are usually students or recent graduates gaining hands-on experience, while Junior Medical Device Engineers are entry-level professionals with some work experience. The internship focuses on learning and support, whereas the junior role involves more responsibility in product development and testing.

What are the most commonly searched types of Medical Device Engineer jobs in Florida?

The most popular types of Medical Device Engineer jobs in Florida are:

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

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

Intern Medical Device Engineer jobs near you
Infographic showing various Intern Medical Device Engineer job openings in Florida as of June 2026, with employment types broken down into 6% Internship, 60% Full Time, 17% Part Time, 6% Temporary, and 11% Contract. Highlights an 88% In-person, 6% Hybrid, and 6% Remote job distribution.

Principal Quality Engineer- Georgia

FloodGate Medical

Tampa, FL • On-site

Full-time

Medical, Life, Retirement, PTO

Posted 5 days ago

Job description

About Zywie
Founded in 2014, Zywie is a founder-led, privately held remote cardiac monitoring company on a mission to transform cardiovascular care. Our flagship product, the ZywieNano™ MCT Patch - the smallest cardiac monitoring patch on the market - delivers up to 30 days of continuous ECG monitoring paired with ZywieAI™, our proprietary AI-driven arrhythmia detection platform.
We have monitored over 500,000 patients, analyzed more than 1 trillion heartbeats, and generated 4.5 million unique clinical notifications. We are profitable, self-funded, and scaling fast - growing our commercial team from 3 to nearly 25 reps in five years. We are now entering the most exciting chapter of our growth: developing and bringing our own proprietary hardware to market. That's where you come in.
The Opportunity
As we transition from a software and services company to a full medical device manufacturer, we're building our Quality organization from the ground up - and we need a Principal Quality Engineer to lead that build. Our first proprietary hardware device is already in active FDA 510(k) submission, with three more devices behind it in our R&D pipeline. This is a foundational, highly visible role: you'll design, implement, and scale our Quality Management System while directly supporting the development and commercialization of our hardware portfolio, reporting to our Sr. Director, Quality & Regulatory Affairs.
What You'll Do
  • Design, implement, and maintain an ISO 13485 and FDA 21 CFR Part 820/QMSR compliant Quality Management System
  • Lead Design Control activities across the product lifecycle, including Design Inputs, Outputs, Verification, Validation, and Design Reviews
  • Lead ISO 14971 Risk Management processes - hazard analysis, FMEA, benefit-risk analysis, and risk management reporting
  • Support software development teams to ensure compliance with IEC 62304, and review software lifecycle and verification documentation
  • Build and manage our supplier quality program, including audits and qualification for our contract manufacturer
  • Lead CAPA, nonconformance, change control, and complaint handling processes
  • Support process validation, manufacturing readiness, and Design Transfer activities
  • Lead implementation and validation of our electronic Quality Management System (eQMS)
  • Prepare the organization for FDA inspections and ISO 13485 certification, including all supporting documentation
  • Partner cross-functionally with Engineering, Clinical, Operations, Regulatory Affairs, and Manufacturing
  • Mentor future Quality Engineers as our organization grows

What You'll Bring
  • Bachelor's degree in Engineering or a related technical discipline; Master's preferred
  • 5+ years of Quality Engineering experience in the medical device industry
  • Demonstrated experience building or significantly enhancing a Quality Management System - not just operating within one
  • Deep knowledge of FDA 21 CFR Part 820/QMSR, ISO 13485, ISO 14971, and IEC 62304
  • Experience supporting Class II and/or Class III medical devices
  • Experience supporting FDA inspections and ISO certification audits
  • Strong Design Controls and Risk Management expertise
  • Experience implementing electronic Quality Management Systems
  • Excellent communication and leadership skills
  • Preferred: experience in startup or high-growth medical device companies, and experience supporting software-enabled devices (SaMD/SiMD), including AI/ML-enabled devices
  • Preferred: ASQ Certified Quality Engineer (CQE), CQA, or equivalent certification

Compensation & Benefits
  • Competitive base salary plus performance bonus, commensurate with experience
  • Full travel reimbursement - flight, hotel, transportation, and daily meal stipend for Atlanta office visits
  • Health Insurance
  • PTO and Holidays
  • 401(k) with company match
  • Life Insurance & AD&D Insurance
  • Direct access to senior leadership and the opportunity to build something that matters
  • A lean, entrepreneurial culture that rewards results and moves fast when the right person is identified

Zywie is an Equal Opportunity Employer. Zywie does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.

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