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Research And Development Engineer Medical Device Jobs in Florida

... medical, and industrial markets. As a Research and Development (R&D) Engineer, you will play a key ... role in driving innovation, new product development, and process improvements that support customer ...

... medical, and industrial markets. As a Research and Development (R&D) Engineer, you will play a key ... role in driving innovation, new product development, and process improvements that support customer ...

KLS Martin has manufactured medical products since 1896, and we have sold our products in the ... Apply Finite Element Analysis (FEA) to understand device risks and failure modes. * Prepare solid ...

KLS Martin has manufactured medical products since 1896, and we have sold our products in the ... Apply Finite Element Analysis (FEA) to understand device risks and failure modes. * Prepare solid ...

... and medical devices. We provide complete interconnect solutions to industries like Aerospace ... The R&D Engineer is responsible for executing engineering deliverables throughout the product ...

Showing results 41-60

Research And Development Engineer Medical Device information

What does a research and development engineer do in the medical device industry?

A Research and Development (R&D) Engineer in the medical device industry is responsible for designing, developing, and testing new medical devices and technologies. They work closely with cross-functional teams to ensure products meet regulatory standards, are safe for patient use, and address clinical needs. Their tasks may include prototyping, conducting experiments, analyzing data, and collaborating with manufacturing teams to bring products from concept to market. R&D Engineers also stay updated on technological advancements and regulatory changes to ensure innovation and compliance.

What are the key skills and qualifications needed to thrive as a research and development engineer in the medical device industry?

To excel as a Research and Development Engineer in Medical Devices, you need a solid background in biomedical engineering or a related field, strong problem-solving skills, and experience with product development cycles. Familiarity with CAD software, prototyping tools, regulatory standards like ISO 13485, and relevant certifications (such as Six Sigma) is highly valued. Excellent teamwork, creativity, and effective communication are crucial soft skills for collaborating across multidisciplinary teams and driving innovation. These competencies ensure the design and launch of safe, effective, and compliant medical devices that improve patient outcomes.

What are some common challenges faced by research and development engineers in the medical device industry?

Research and Development Engineers in the medical device industry often face challenges such as navigating complex regulatory requirements, managing tight project timelines while ensuring product safety and efficacy, and collaborating with cross-functional teams like quality assurance and clinical affairs. Additionally, adapting to rapid technological advancements and integrating feedback from clinicians and end-users into the design process can be demanding. These challenges require strong problem-solving skills, adaptability, and effective communication to deliver innovative and compliant medical devices.

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

AspectResearch And Development Engineer Medical DeviceQuality Assurance Engineer Medical Device
Primary FocusDesigning, developing, and testing new medical device productsEnsuring products meet quality standards and regulatory requirements
Required CredentialsEngineering degree, knowledge of product developmentEngineering or science degree, knowledge of quality systems
Work EnvironmentResearch labs, product development teamsManufacturing facilities, quality control departments
Industry UsageInvolved in innovation and product creationInvolved in compliance, validation, and process improvement

While both roles require engineering knowledge and are integral to the medical device industry, Research And Development Engineers focus on creating and testing new products, whereas Quality Assurance Engineers ensure these products meet safety and quality standards throughout production.

What are popular job titles related to Research And Development Engineer Medical Device jobs in Florida?

For Research And Development Engineer Medical Device jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Research And Development Engineer Medical Device jobs in Florida look for?

The top searched job categories for Research And Development Engineer Medical Device jobs in Florida are:

What cities in Florida are hiring for Research And Development Engineer Medical Device jobs?

Cities in Florida with the most Research And Development Engineer Medical Device job openings:

Full-time

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Job description

SUMMARY:

Amphenol Cable & Interconnect Technologies (ACIT) is a leading provider of advanced cable, interconnect, and connectivity solutions serving the aerospace, defense, medical, and industrial markets. As a Research and Development (R&D) Engineer, you will play a key role in driving innovation, new product development, and process improvements that support customer requirements and business objectives.

The R&D Engineer is responsible for executing engineering deliverables throughout the product development lifecycle, including concept development, design, testing, validation, and manufacturing implementation. This role applies sound engineering principles to develop products and processes that meet customer, quality, and operational requirements while supporting efficient project execution through strong technical and project management skills. The position requires close collaboration with cross-functional teams including engineering, product management, operations, quality, and sales, with a focus on innovation, continuous improvement, and customer satisfaction

ESSENTIAL JOB FUNCTIONS

  • Serve as a core team member in Product and Process Risk Analysis and lead multiple NPD projects through the Stage Gate process, ensuring completion of key deliverables and milestones.
  • Own proof-of-concept builds and support prototype development, including setup and operation of manufacturing equipment.
  • Plan, execute, and document engineering activities, including test data, process setups, and project status reporting.
  • Lead and manage capital equipment projects, including development of capital expenditure (ACE) requests.
  • Collaborate cross-functionally with engineering, production, product management, and sales teams to support product development and manufacturability.
  • Interface with internal and external customers to define technical requirements, establish test plans, and support product selection and application needs.
  • Support product testing, validation, and qualification activities; analyze data to drive troubleshooting and continuous improvement.
  • Develop cost estimates, tooling requirements, and manufacturing documentation (e.g., work instructions, jigs, fixtures).
  • Monitor industry trends and contribute to innovation and new product development strategies.
  • Support production and process engineering teams while promoting safety, quality, and operational excellence.
  • Utilize and support operational systems and tools (e.g., LabVIEW, SAP, Power BI).
  • Mentor and guide engineering technicians to ensure successful project execution.
  • Other duties as required in support of the department and the company

SUPERVISOR RESPONSIBILITIES

Capable of leading projects and assigning resources for successful completion.

 

QUALIFICATIONS

 

  • Bachelor's degree in Electrical Engineering preferred; Mechanical Engineering or a related engineering discipline will be considered with relevant product development and hands-on engineering experience.
  • Experience in a manufacturing environment in a technical or engineering role; connectors and assemblies preferred.
  • Proficiency in CAD software (e.g., SolidWorks, AutoCAD, CATIA, Creo) with experience in fixture or machine design.
  • Experience with data acquisition and analysis tools (e.g., LabVIEW, SAP, Excel), including DOE and statistical analysis.
  • Strong project management skills with experience managing multiple priorities, including equipment selection and capital justification processes.
  • Solid understanding of engineering drawings, specifications, and technical documentation, with the ability to write reports and protocols.
  • Effective communication and collaboration skills across cross-functional teams, customers, and suppliers; broad engineering knowledge (electrical, mechanical, industrial), with experience in regulated industries (e.g., aerospace, medical/FDA) as a plus.

 

CERTIFICATES, LICENSES, REGISTRATIONS

  • Engineering degree with a broad engineering knowledge across electrical, mechanical, and industrial disciplines, with specialization in at least one area.

LANGUAGE REQUIREMENTS

  • Proficiency in English sufficient to understand technical documentation, safety procedures, and work instructions, and to interpret information in written, verbal, diagrammatic, and schedule formats.
  • Ability to communicate effectively in written and verbal formats, including preparing clear technical reports and collaborating with cross-functional teams, customers, and suppliers.

MATHEMATICAL SKILLS

  • Ability to apply statistical methods, including Design of Experiments (DOE), to analyze and interpret data, assess variability and process capability, and support troubleshooting, optimization, and product development.
  • Ability to perform engineering calculations (e.g., cost, tolerances, performance) and utilize software tools (e.g., Excel or similar) for data analysis, modeling, and reporting.

 

PHYSICAL DEMANDS

The physical requirements outlined below indicate those necessary to fulfill this position's core responsibilities. While performing job duties, the employee will regularly engage in activities such as using hands to finger, handle, or feel, and communicating verbally. Additionally, the employee will frequently need to reach with hands and arms while standing and walking as part of the role. Occasional lifting and movement of objects weighing up to fifty (50) pounds and using a ladder may be required. This position also demands specific vision capabilities, including close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus. Reasonable accommodation will be provided according to ADA regulations to enable individuals with disabilities to perform the job's essential functions.

WORK ENVIRONMENT

A work environment in a manufacturing plant is the physical and social setting where goods production occurs. Depending on the type of product, process, and plant, the work environment may vary in terms of noise, temperature, safety, and demand. Common characteristics of a work environment in a manufacturing plant are the use of machinery and exposure to hazards such as chemicals, heat, dust, or noise, with a culture of teamwork, communication, and continuous improvement.

 

ENVIRONMENTAL POLICY

Amphenol-CIT is fully committed to minimizing the environmental impact of its operations, activities, and products. To achieve this, we adhere to all applicable environmental regulations and laws, prevent pollution, and continuously improve our environmental performance in all our global operations. This is possible through an Environmental Management System that provides a framework for setting and reviewing our environmental objectives and targets. We aim to identify and reduce any negative environmental impact our business activities may have.

 

PERSONAL PROTECTIVE EQUIPMENT REQUIREMENTS

  • ASTM F–2412–2005, ANSI Z41–1999, or ANSI Z41–1991 rated safety toe shoes in specific areas.
  • Clear ANSI Z87.1 safety-rated glasses in specific areas.
  • Hearing protection in specific locations.
  • Ability to compile with JSA in specific areas.

 

EXPORT COMPLIANCE DISCLAIMER

This position includes access or potential access to ITAR and EAR (Export Administration Regulations) technical data. Therefore, candidates must qualify as US Persons, defined as US Citizens or Permanent Residents (Green Card Holders).

TRAVEL

Approximately 10% of travel is expected.