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Medical Device Startup Jobs in Arizona (NOW HIRING)

LotusWorks

Area Coordinator

Chandler, AZ · On-site

... Biologics, Medical Device and Data Centre sectors. Our team of Engineering and Technical ... startup phases. Responsibilities: * Coordinate daily construction activities within an assigned ...

LotusWorks

I&C Field Engineer

Chandler, AZ · On-site

... Biologics, Medical Device and Data Centre sectors. Our team of Engineering and Technical ... system startup, loop checks, functional testing, troubleshooting, commissioning, and turnover ...

LotusWorks

I&C Superintendent

Chandler, AZ · On-site

... Biologics, Medical Device and Data Centre sectors. Our team of Engineering and Technical ... Support startup and commissioning activities for utilities, equipment, and safety systems * Track ...

LotusWorks

Master Chiller Mechanic

Chandler, AZ · On-site

... Biologics, Medical Device and Data Centre sectors. Our team of Engineering and Technical ... Support seasonal startup and shutdown activities for chillers and associated utility systems.

Foresight Technologies Inc

Systems Engineer

Tempe, AZ · On-site

Support equipment validation, commissioning, and startup activities. * Participate in new product ... Experience in semiconductor, aerospace, medical device, or precision manufacturing. * Familiarity ...

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Showing results 1-20

All JobsMedical Device Startup JobsMedical Device Startup Jobs in Arizona

Medical Device Startup information

See Arizona salary details

$19

$34

$65

How much do medical device startup jobs pay per hour?

As of Jul 28, 2026, the average hourly pay for medical device startup in Arizona is $34.22, according to ZipRecruiter salary data. Most workers in this role earn between $23.08 and $42.79 per hour, depending on experience, location, and employer.

What is the difference between Medical Device Startup vs Medical Device Engineer?

AspectMedical Device StartupMedical Device Engineer
Required CredentialsTypically requires engineering degree, certifications varyRequires engineering degree, often with specific certifications in biomedical or mechanical engineering
Work EnvironmentFast-paced, innovative startup setting, often small teamsDesign, develop, and test medical devices, usually in corporate or R&D labs
Employer & Industry UsageStartups in medical device industry, early-stage companiesEstablished companies, R&D departments, or startups
Common Search & Comparison IntentUnderstanding roles in startups, career optionsJob responsibilities, qualifications, career path

Medical Device Startup roles focus on innovation, product development, and often require versatile skills in a dynamic environment. Medical Device Engineers are specialized professionals responsible for designing and testing devices, typically within established or startup companies. While both roles require engineering credentials, startups emphasize adaptability and entrepreneurial spirit, whereas engineers focus on technical expertise and product quality.

What is a medical device startup?

A medical device startup is a company in its early stages that focuses on developing, manufacturing, and bringing innovative medical devices to market. These startups often work on new technologies or improvements to existing devices, aiming to address unmet medical needs or improve patient outcomes. They typically operate in a high-regulation environment and may seek funding from investors, grants, or partnerships to support research, development, and commercialization efforts. Success in this field requires multidisciplinary expertise, including engineering, regulatory affairs, and clinical knowledge.

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

To thrive in a medical device startup, you need a solid background in biomedical engineering, product development, and regulatory compliance, often supported by relevant degrees or experience in healthcare technology. Familiarity with FDA regulations, CAD design software, and project management tools like Jira or Asana is typically required. Strong collaboration, adaptability, and entrepreneurial problem-solving are essential soft skills in this dynamic environment. These skills and qualities are vital for navigating rapid innovation cycles, ensuring regulatory approval, and driving successful product launches in a competitive market.

What Are Jobs at a Medical Device Startup?

Jobs at a medical device startup include roles in research and development, sales, information technology, software development, and customer service. Working at a medical device startup in research and development, you collaborate with teams to design studies, perform research, and devise training materials for products. Your end goal is to help develop new products. As a sales representative, you promote and sell medical equipment, educate clients on the benefits of products, and respond to questions and concerns. Software and IT jobs at a medical device startup involve responsibilities like troubleshooting technical problems, diagnosing and repairing computer systems, creating databases, evaluating processes, and maintaining and utilizing medical imaging equipment.

What are the common challenges faced when working in a medical device startup environment?

Working in a medical device startup often involves navigating a fast-paced, dynamic environment where priorities can shift rapidly. Team members typically wear multiple hats, balancing product development with strict regulatory requirements and limited resources. Collaboration across engineering, clinical, and business teams is essential, as everyone works together to meet ambitious milestones and bring innovative products to market. Despite these challenges, the role provides unique opportunities to make a tangible impact and grow professionally within a close-knit, innovative team.
More about Medical Device Startup jobs
What are popular job titles related to Medical Device Startup jobs in Arizona? For Medical Device Startup jobs in Arizona, the most frequently searched job titles are:
What job categories do people searching Medical Device Startup jobs in Arizona look for? The top searched job categories for Medical Device Startup jobs in Arizona are:
What cities in Arizona are hiring for Medical Device Startup jobs? Cities in Arizona with the most Medical Device Startup job openings:
Medical Device Startup jobs near you
Infographic showing various Medical Device Startup job openings in Arizona as of July 2026, with employment types broken down into 81% Full Time, 12% Part Time, and 7% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $71,182 per year, or $34.2 per hour.
Clinical Research, Regulatory Associate

Clinical Research, Regulatory Associate

Castle Biosciences, Inc

Phoenix, AZ • On-site

Full-time

Medical, Retirement, PTO

Posted 12 days ago

Job description

Castle Biosciences Earns "Top Workplaces USA Award" for Phoenix, Pittsburgh, and Friendswood!

Learn more at www.CastleBiosciences.com

Castle Biosciences Inc. is growing, and we are looking to hire a full-time Clinical Research, Regulatory Associate working from our Phoenix, AZ office location, with a start date of August 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 A Regulatory Associate,

The Regulatory Associate organizes and supports the daytoday regulatory activities for assigned clinical studies. This role coordinates site outreach, study and site startup activities, IRB submissions, and ongoing electronic Trial Master File (TMF) management. A typical day includes collecting and reviewing critical regulatory documents to support study startup, maintenance, and closeout, ensuring documents submitted by CRAs are complete, compliant, and filed accurately in CTMS or TMF systems. The Regulatory Associate regularly reviews TMF inventories to identify missing, incomplete, or expiring documents and communicates gaps to study team members. Serving as a regulatory resource, this role supports preparation of regulatory submissions and advises study teams on Good Clinical Practice (GCP), FDA, and applicable regulatory requirements.

REQUIREMENTS

  • Bachelor's degree in a scientific, engineering, regulatory, or related field preferred, or demonstrated equivalent experience supporting medical device regulatory activities
  • Minimum of 1 year of experience in medical device regulatory affairs, clinical research, or related regulated industry required
  • Familiarity with medical device product development lifecycle, including design controls and risk management processes
  • Working knowledge of U.S. (e.g., 21 CFR 820, 21 CFR 812), European (e.g., EU MDR 2017/745), and/or other global medical device regulations and standards (e.g., ISO 13485, ISO 14971, ISO 14155)
  • Experience supporting regulatory submissions (e.g., 510(k), De Novo, Technical Documentation, IDE) preferred

*Please see the full job description at the end of the job ad.

SCHEDULE

  • Monday-Friday, 40 hour work week, working on-site from our Phoenix, AZ office, flexible hours between 7am-5pm.

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!

Castle Biosciences Awards and Research Developments!

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 ReasonableAccommodationsRequest@castlebiosciences.com.

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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