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Research And Development Engineer Medical Device Jobs in Arizona

Comrise

R&D Engineer Medical Device

Tempe, AZ · On-site

$50 - $55/hr

Follow R&D procedures like design controls and risk management, per the Quality Management System ... Vascular device engineering preferred Technical ability to develop and optimize designs for medical ...

New

Three Point Solutions

Principal R&D Engineer

Tempe, AZ · On-site

$55 - $65/hr

Medical Device Manufacturing Company Duration: 8.5 Months (Possibility of Extension) Location: Tempe, AZ 85281 Shift: 1st Shift Description: * Lead the development, validation, and optimization of ...

Innovative Health LLC

Sr. R&D Engineer

Scottsdale, AZ · On-site

$101K - $139K/yr

The Senior R&D Engineer role is responsible for designing, developing, validating, and implementing ... Essential Duties and Responsibilities: • Lead development of advanced medical device reprocessing ...

Innovative Health

Sr. R&D Engineer

Scottsdale, AZ

$105K - $144K/yr

The Senior R&D Engineer role is responsible for designing, developing, validating, and implementing ... Essential Duties and Responsibilities: · Lead development of advanced medical device reprocessing ...

Innovative Health LLC

Sr. R&D Engineer

Scottsdale, AZ · On-site

$101K - $139K/yr

The Senior R&D Engineer role is responsible for designing, developing, validating, and implementing ... Essential Duties and Responsibilities: · Lead development of advanced medical device reprocessing ...

R&D Partners

Research Associate II

Tucson, AZ · On-site

$27/hr

... engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies. R&D Partners is an equal-opportunity employer. Company ...

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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 Arizona?

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

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

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

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

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

Research And Development Engineer Medical Device jobs near you

R&D Engineer Medical Device

Comrise

Tempe, AZ • On-site

$50 - $55/hr

Contractor

Posted yesterday

New

Job description

This role will be Mon-Fri 8:00am – 5:00pm.  It will be hybrid with the expectation of at least three days on site in Tempe.
 
Designs, validates and brings new products to market. Specifies precise new product functional requirements; designs, tests and integrates components to produce final designs; and evaluates the design's overall effectiveness, cost, reliability and safety. Designs, develops, executes and evaluates fitness-for-use testing, product specifications and process validation plans; creates and reviews material part specifications and bills of materials. Collaborates with internal manufacturing partners, contract manufacturers, designers and product specialists to optimize designs for manufacturability. Utilizes CAD (Computer Aided Design) or CAE (Computer Aided Engineering) systems to model new designs and produce detailed engineering drawings.
This is an individual contributor role that requires the use of judgement in applying professional expertise and is expected to work independently with minimal supervision. Roles typically require a university degree or an extensive amount of practical knowledge gained through experience. Job requires an understanding and application of procedures and concepts of own discipline. The job requires the ability to make judgements based on practice and previous experience. This job typically requires a degree or equivalent and no experience.
KEY AREAS OF RESPONSIBILITY: What you will do:
Technical Responsibilities:
• Research, design, develop, modify, and verify components and systems for medical devices with minimal supervision.
• Translate user needs to design inputs/ specifications and produce system-level designs.
• Develop and analyze solutions, prototyping one or more options to provide proof of concept.
• Apply fundamental and some advanced concepts, practices and procedures for problem solving.
• Support problem solving, root cause analysis, identify potential solutions, and evaluate them against requirements.
• Develop bench testing methods, conduct measurement system analysis, and develop DOE.
• Conduct research and studies to support product design.
Business Responsibilities:
• Demonstrate advanced understanding of customer needs and design inputs.
• Demonstrate proficiency with product’s intended use and clinical procedures.
• Learn how the financial models are constructed
• Support Voice of Customer sessions internally and with clinicians to develop an understanding of customer needs
• Apply understanding of customer needs to development of robust and appropriate design inputs.
• Understand the product’s intended use and clinical procedures.
• Apply understanding of the impact of design decisions on production metrics (COGS, yield, etc.).
Med Device Compliance:
• Follow fundamental industry standards, design requirements and test strategies which apply to regulatory requirements.
• Independently create or refine engineering documentation, such as the Design History file.
• Follow R&D procedures like design controls and risk management, per the Quality Management System.
 
General Responsibilities:
• Under minimal supervision, work with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success.
• Quickly process and assimilate procedures, policies, processes, systems, and technology required.
• Work on complex problems, applying advanced experience and learnings.
• Demonstrate ownership and prioritize work with minimal supervision.
• Works as key member of the team, collaborating with others and solidifying relationships.
• Support multifunctional teams to and execute segments of projects through the design, development, and launch process.
• Deliver high quality results with passion, energy and drive to meet business priorities.
• Collaborate with cross-functional teams to build partnership to achieve business objectives.
 
PREFERRED QUALIFICATIONS: What you will need (strongly desired):
Technical Skills:
• Vascular device engineering preferred
Technical ability to develop and optimize designs for medical device assemblies, incorporating DFM principles and clinical feedback and knowledge.
• Ability to communicate basic plans and technical information to team members, leaders, and project managers
• Technical knowledge in creating product test fixtures and developing test methods for verification and validation activities
• Fundamental knowledge and understanding of engineering practices, tools, and design principles within a regulated environment.
• Demonstrated ability to influence and drive results through others.
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About Comrise

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With over 38 years of staffing and business experience, Comrise continues to lead by example. We provide personalized and customized business solutions for all your recruiting and talent. Headuartered in New Jersey since 1984, Comrise is a staffing, consulting and enhanced search technology company. For over 38 years, we have delighted our clients and consultants by focusing on customer satisfaction, innovation, and flexible workforce solutions! With locations in the U.S, China, and Southeast Asia, we provide high-quality executive search, temporary assignments, temporary to permanent opportunities and cross border placement services.

Industry

It services

Company size

201 - 500 Employees

Headquarters location

Woodbridge, NJ, US

Year founded

1984

Social media

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