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Intern Medical Device Engineer Jobs in Florida (NOW HIRING)

Currently pursuing a Bachelor's, Master's, or PhD degree in Biomedical Engineering, Mechanical ... device research within Scientific Affairs. Location 111 West Oak Ave., Tampa, FL 33602 #LI-AC1 ...

Currently pursuing a Bachelor's, Master's, or PhD degree in Biomedical Engineering, Mechanical ... device research within Scientific Affairs. Location 111 West Oak Ave., Tampa, FL 33602 #LI-AC1 ...

Currently pursuing a Bachelor's, Master's, or PhD degree in Biomedical Engineering, Mechanical ... device research within Scientific Affairs. Location 111 West Oak Ave., Tampa, FL 33602 #LI-AC1 ...

Intern - Eng Test Lab

Gainesville, FL · On-site

$15 - $19.50/hr

Intern - Eng Test Lab Department: Engineering, Extremities Employment Type: Full Time Location ... Apply engineering acumen to evaluate impact of revisions to technical standards on medical device ...

Strong interest in manufacturing engineering within the tissue space, as well as manufacturing ... or medical device/biotechnology industries * Demonstrated ability to independently research and ...

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Intern Medical Device Engineer information

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 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 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 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 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:
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.

Senior Device Engineer, Pharmaceutical R&D

Transpire BIO Inc.

Weston, FL

$99K - $136K/yr

Full-time

Re-posted 24 days ago


Job description

Position Summary

The Senior Device Engineer is responsible for device engineering activities in the context of pharmaceutical research and development (R&D). The device mechanical engineer will be responsible for early to late-stage device development activities and commercialization of drug-device combination products. The Device engineer will be responsible for design, prototyping, technical analysis, and testing of orally inhaled and nasal drug products (OINDPs). Provide device engineering leadership in the direction, initiation, planning, coordination, implementation, execution, control, and completion of specific device project(s) ensuring consistency with organizational strategy, commitments, and goals. The device engineer will need to ensure that the device designs meet user needs, regulatory and quality requirements, and consider manufacturability. This is a hands-on position which requires daily tactical responsibilities leading up to strategic decisions.

Essential Duties and Responsibilities

  • In support of the Product Development Teams, provide technical leadership in the device development area.
  • Execute design and development of orally inhaled and nasal drug products (OINDPs) following design controls.
  • Lead and execute analysis for device and product characterization, design feasibility, and design verification.
  • Lead and execute technical analyses including statistical analysis and tolerance analysis.
  • Lead root cause investigations.
  • Support scale-up and commercialization efforts.
  • Document studies and author documents per US FDA, EMA, MHRA and other global health authority requirements.
  • Interface and lead activities with third party contract research, development, and manufacturing organizations.
  • Contribute towards and maintain device design history files (DHF).
  • Document standard operating procedures (SOPs) for design controls in the context of pharmaceutical drug-device combination products.
  • Provide project updates/reporting through program governance.
  • Provide leadership and support for inter-site best practices (technology transfer, process validation, etc.) and phase appropriate guidelines and policies.
  • Execute project strategy, priorities, and milestones ensuring visibility and accountability.
  • Proactively lead with integrity and engage cross functional project teams and stakeholders.
  • Support organizational / departmental initiatives.
  • Prepare and conduct presentations to all levels of the organization which may include project technical and budgetary information.

Required Qualifications

  • A M.S, in Mechanical Engineering, Electrical Engineering, Material Sciences or related discipline with 7 to 10 years, B.S. with 10 to 14 years device development experience in pharmaceutical or related field.
  • Experience with device development in the context of pharmaceutical R&D and product development is a must to have.
  • Must possess expert knowledge of mechanical design with preference for SolidWorks.
  • Must possess expert knowledge of tools to conduct statistical and tolerance analysis.
  • Must possess knowledge of manufacturing processes including injection molding and metal machining processes.
  • Must possess knowledge of regulations and standards including US 21 CFR Part 820, ISO 13485, ISO 14971, ISO 10993, EU MDR etc.
  • Experience with device assembly processes including manual, semi-automated and/or commercial scale automated processes is a plus.
  • Experience in development of orally inhaled and nasal drug products (OINDPs) is a plus.
  • Experience in mold tool design, optimization and qualification is a plus to have.
  • Experience with Notified Bodies and CE marking is a plus.
  • Strong English language skills including writing ability and oral communication.
  • Demonstrates good judgment as well as cultural, social, and environmental awareness.

Preferred Qualifications

  • Experience in a regulated laboratory (pharma, biotech, medical device, mechanical, or environmental)
  • Knowledge of GMP, GLP, or ISO standards

Why Join Us?

We are a fast-growing pharmaceutical startup dedicated to innovation and improving patient outcomes. Join us to gain hands-on experience in a growing pharmaceutical business, get exposure to various functions with opportunities for career development and work in a collaborative and supportive work environment.