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Medical Device Research And Development Jobs in Florida

Medical Device Rep

Boca Raton, FL · On-site

$82K - $113K/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 ...

Medical Device Rep

Sarasota, FL · On-site

$82K - $113K/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 ...

Sr. Engineer, R&D (Biomaterials)

Tampa, FL

$98K - $135K/yr

Job Summary of the Sr. Engineer, R&D The Sr. Engineer, Research & Development, is an experienced ... Minimum of 5 years of experience in the medical device or pharmaceutical industry. Product ...

Sr. Engineer, R&D

Tampa, FL · On-site

$98K - $135K/yr

Job Summary of the Sr. Engineer, R&D The Sr. Engineer, Research & Development, is an experienced ... Minimum of 5 years of experience in the medical device or pharmaceutical industry. Product ...

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 ...

Sr. Engineer, R&D (Biomaterials)

Tampa, FL · On-site

$98K - $135K/yr

Job Summary of the Sr. Engineer, R&D The Sr. Engineer, Research & Development, is an experienced ... Minimum of 5 years of experience in the medical device or pharmaceutical industry. Product ...

Sr. Engineer, R&D (Biomaterials)

Tampa, FL · On-site

$98K - $135K/yr

Job Summary of the Sr. Engineer, R&D The Sr. Engineer, Research & Development, is an experienced ... Minimum of 5 years of experience in the medical device or pharmaceutical industry. Product ...

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 ...

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Showing results 1-20

Medical Device Research And Development information

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

To thrive in Medical Device Research and Development, you need a solid background in engineering or life sciences, along with experience in product design and knowledge of regulatory standards. Familiarity with CAD software, prototyping tools, and compliance systems such as ISO 13485 or FDA regulations is typically required. Strong problem-solving skills, creativity, and effective teamwork set standout professionals apart in this field. These skills and qualities are crucial to ensure innovative, safe, and compliant medical devices that meet both clinical needs and regulatory requirements.

What are some typical challenges faced by professionals in medical device research and development, and how can these be managed?

Professionals in Medical Device Research and Development often encounter challenges such as navigating complex regulatory requirements, balancing innovation with safety, and coordinating cross-functional teams. Managing these challenges involves staying current with FDA and international regulations, fostering open communication between engineering, clinical, and regulatory teams, and maintaining rigorous documentation throughout the development process. Strong project management skills and a collaborative mindset are key to overcoming these obstacles and ensuring successful product development.

What is medical device research and development?

Medical device research and development (R&D) is the process of designing, creating, testing, and improving medical devices used for diagnosing, treating, or preventing health conditions. This field combines engineering, biology, and medicine to develop innovative tools ranging from simple instruments to complex implantable devices. Professionals in this area work on everything from concept development and prototyping to clinical trials and regulatory approval. Their work ensures that medical devices are safe, effective, and meet strict regulatory standards before reaching patients.

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

AspectMedical Device Research And DevelopmentMedical Device Quality Assurance
CredentialsEngineering degrees, certifications in R&DQuality certifications, regulatory training
Work EnvironmentLabs, design teams, product developmentInspection facilities, compliance departments
Employer & Industry UsageManufacturers, biotech firms, innovation labsRegulatory agencies, manufacturing companies
Search & Comparison IntentInnovation, product development, prototypingCompliance, testing, product validation

Medical Device Research And Development focuses on designing and developing new medical devices, emphasizing innovation and prototyping. In contrast, Medical Device Quality Assurance ensures products meet safety and regulatory standards through testing and compliance. Both roles are essential in the medical device industry but serve different stages of the product lifecycle.

What job categories do people searching Medical Device Research And Development jobs in Florida look for? The top searched job categories for Medical Device Research And Development jobs in Florida are:
What cities in Florida are hiring for Medical Device Research And Development jobs? Cities in Florida with the most Medical Device Research And Development job openings:
Infographic showing various Medical Device Research And Development 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.

Senior Device Engineer, Pharmaceutical R&D

Transpire BIO Inc.

Weston, FL • On-site

$99K - $136K/yr

Full-time

Re-posted 29 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.