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Medical Device Research And Development Jobs in Arizona

Becton, Dickinson and Company

R&D Engineer III

Tempe, AZ · On-site

Designs, develops and implements products and processes of a medical device, translating intangible ... Mentor/coach R&D technicians through activities like process development, R&D materials/inventory ...

Becton, Dickinson and Company

R&D Engineer III

Tempe, AZ · On-site

Designs, develops and implements products and processes of a medical device, translating intangible ... Mentor/coach R&D technicians through activities like process development, R&D materials/inventory ...

System One

Device Design Engineer

Tempe, AZ · On-site

Research, design, develop, modify, and verify components and systems for medical devices with ... Apply understanding of customer needs to development of robust and appropriate design inputs.

System One

Device Design Engineer

Tempe, AZ · On-site

Research, design, develop, modify, and verify components and systems for medical devices with ... Apply understanding of customer needs to development of robust and appropriate design inputs.

System One

Device Design Engineer

Tempe, AZ · On-site

Research, design, develop, modify, and verify components and systems for medical devices with ... Apply understanding of customer needs to development of robust and appropriate design inputs.

Sitka Inc.

Histology Specialist

Tempe, AZ · On-site

$65 - $85/hr

... medical device research and development. The successful applicant will have demonstrated the ability to be highly competent in performing histology lab procedures and operating/maintaining lab ...

BEPC INC

Be Seen First

Research Associate II Assay Development

Tucson, AZ · On-site

$25 - $27/hr

Benefits include medical, dental, vision, and life insurance Pay Rate: $25.00 - $27.00/hour ... This role will support research, development, and manufacturing laboratory experimentation ...

BEPC INC

Be Seen First

Research Associate II Assay Development

Tucson, AZ · On-site

$25 - $27/hr

Benefits include medical, dental, vision, and life insurance Pay Rate: $25.00 - $27.00/hour ... This role will support research, development, and manufacturing laboratory experimentation ...

Bdx

BD Engineering Development Program

Tempe, AZ · On-site

... medical device instrumentation and applications. A successful candidate will work under the supervision of an R&D manager and team to develop and maintain medical technology and devices. They work to ...

Stryker Group

Senior Operations Manager

Phoenix, AZ · On-site

$136 - $226/hr

... medical device environment. This position is responsible for leading manufacturing, planning ... Partner with Quality, Engineering, Regulatory Affairs, Research & Development, Customer Service ...

Viant

Commercial Development Manager

Tempe, AZ · On-site

Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With ...

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All JobsMedical Device Research And Development JobsMedical Device Research And Development Jobs in Arizona

Medical Device Research And Development information

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 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 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 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 are popular job titles related to Medical Device Research And Development jobs in Arizona?

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

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

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

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

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

Medical Device Research And Development jobs near you
Infographic showing various Medical Device Research And Development job openings in Arizona as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 14% Part Time, 2% Temporary, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution.

Clinical Research, Clinical Safety Manager

Castle Biosciences

Phoenix, AZ • On-site

Full-time

Medical, Retirement, PTO

Re-posted 16 hours ago

Job description

Learn more at
Castle Biosciences Inc. is growing, and we are looking to hire a full-time Clinical Research, Clinical Safety Manager working from our Phoenix, AZ, Friendswood, TX or Pittsburgh, PA office location, with a start date of September 1, 2026.
Why Castle Biosciences?
Exceptional Benefits Package:
  • Excellent Annual Salary + 20% Bonus Potential
  • 20 Accrued PTO Days Annually + 10 Paid Holidays
  • 401K with 100% Company Match up to 6%
  • 3 Health Care Plan Options + Company HSA Contribution
  • Company Stock Grant Upon Hire

A DAY IN THE LIFE OF AN Clinical Safety Manager
The Clinical Research Safety Manager is responsible for establishing, implementing, and continuously improving clinical research safety processes for a laboratory-developed test (LDT) and medical device organization while ensuring compliance with applicable regulations, Company policies, and Standard Operating Procedures (SOPs). This role serves as the operational safety lead for company-sponsored clinical studies, overseeing safety planning, adverse event management, risk assessments, safety reporting, and regulatory documentation for FDA-regulated LDT, IVD, and medical device studies. The position partners with cross-functional teams to ensure participant safety, regulatory compliance, inspection readiness, and alignment between clinical safety activities, quality systems, and post-market processes. This individual contributor role also supports the development of safety processes, study documentation, and training while providing support as directed by leadership and contributing to the growth of the clinical research safety function.
REQUIRED QUALIFICATIONS
  • Bachelor's degree in life sciences, nursing, clinical research, biomedical sciences, regulatory/quality, public health, or related field.
  • 5+ years of clinical research, clinical safety, medical device/IVD, diagnostics, regulatory, quality, or related experience in a regulated healthcare environment.
  • Demonstrated experience supporting sponsor-led clinical studies, preferably device/IVD/LDT studies, including protocol review, safety reporting pathways, IRB/EC interactions, and study documentation.
  • Working knowledge of FDA clinical research and medical device requirements, including 21 CFR Parts 803, 812, and 820 and applicable safety/reporting expectations.
  • Experience evaluating and documenting adverse events, serious adverse events, unanticipated problems, unanticipated adverse device effects, protocol-defined events, deviations, and safety issues.

*Please see the full job description at the end of the job ad.
SCHEDULE
  • Monday-Friday, 40 hours per week, working from our Phoenix, AZ, Friendswood, TX or Pittsburgh, PA office locations.
  • Occasional overnight travel, up to 10%, may be required to support site engagement, audits/inspections, study meetings, training, or conferences.

READY TO JOIN OUR BIOTECH TEAM?
We truly appreciate your time. If this feels like the right opportunity for you, we'd love for you to complete our mobile-friendly application. We're excited to learn more about you and look forward to connecting soon!
WORK AUTHORIZATION
All candidates must be legally authorized to work in the United States. Currently, Castle Biosciences does not sponsor H-1B visas, OPT, or employment-related visas.
ABOUT CASTLE BIOSCIENCES INC.
At Castle, it all comes down to people. After all, disease doesn't just happen - it happens to people. We believe that disease management and treatment decisions can be better informed through a person's unique biology, which is revealed through the scientific rigor of our innovative, laboratory-developed tests. We are committed to empowering healthcare providers and patients with the goal of improved outcomes.
Every employee at Castle has an impact on patient care, and we work to ensure that everyone finds their work to be both challenging and rewarding. We behave with integrity and treat our colleagues with respect and kindness. Our culture fosters an environment of trust, transparency, and collaboration. We prioritize and encourage internal growth and professional development.
Castle Biosciences is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities.
If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please e-mail .
This email was created exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only messages left for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response.
** No third-party recruiters, please

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