1

Medical Device Manufacturing Engineer Jobs in Arizona

Directs the engineering teams and activities for new product introduction, commercial and clinical ... Acts as site Subject Matter Expert for medical device manufacturing on site across all functions ...

Directs the engineering teams and activities for new product introduction, commercial and clinical ... Acts as site Subject Matter Expert for medical device manufacturing on site across all functions ...

Directs the engineering teams and activities for new product introduction, commercial and clinical ... Acts as site Subject Matter Expert for medical device manufacturing on site across all functions ...

IntePros is seeking an experienced Mold Maker to support a medical device/manufacturing client in ... Read and interpret engineering drawings and mechanical documentation * Inspect components using ...

Bachelor's degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering ... Minimum 2 years of experience in a medical device or regulated manufacturing environment.

Bachelor's degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering ... Minimum 2 years of experience in a medical device or regulated manufacturing environment.

Be Seen First

Medical Device Assembler

Marana, AZ · On-site

$17 - $18.08/hr

Medical Device Assembler Location: Marana, AZ 85653 Employment Type: W2 Contract - 12 Months with ... technology, engineering, manufacturing, and project management. At BEPC, we are driven by ...

next page

Showing results 1-20

Medical Device Manufacturing Engineer information

See Arizona salary details

$44.3K

$79.8K

$111.8K

How much do medical device manufacturing engineer jobs pay per year?

As of Sep 3, 2026, the average yearly pay for medical device manufacturing engineer in Arizona is $79,782.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,000.00 and $87,600.00 per year, depending on experience, location, and employer.

What does a medical device manufacturing engineer do?

A Medical Device Manufacturing Engineer is responsible for designing, developing, and optimizing manufacturing processes for medical devices. They ensure that products are produced efficiently, safely, and in compliance with regulatory standards such as FDA or ISO guidelines. Their work involves collaborating with design teams, troubleshooting production issues, implementing quality control procedures, and continuously improving manufacturing methods to enhance product quality. Ultimately, they play a key role in bringing safe and effective medical devices to market.

What are the key skills and qualifications needed to thrive as a medical device manufacturing engineer?

To excel as a Medical Device Manufacturing Engineer, you need a solid background in engineering principles, manufacturing processes, and regulatory compliance, typically supported by a degree in biomedical, mechanical, or industrial engineering. Familiarity with CAD software, Six Sigma/Lean methodologies, and knowledge of FDA or ISO 13485 standards is essential. Strong problem-solving, teamwork, and communication skills help manage cross-functional projects and ensure product quality. These competencies are crucial for developing safe, effective devices in a highly regulated industry where precision and compliance are paramount.

What are some common challenges faced by medical device manufacturing engineers during product development?

Medical Device Manufacturing Engineers often encounter challenges in balancing strict regulatory compliance with efficient production processes. Adapting to frequent design changes, ensuring high product quality, and validating manufacturing processes are crucial tasks. Additionally, they collaborate closely with cross-functional teams—including quality assurance, R&D, and supply chain—to troubleshoot production issues and implement improvements. Addressing these challenges requires strong problem-solving skills and a keen attention to detail.

What is the difference between Medical Device Manufacturing Engineer vs Quality Assurance Engineer?

AspectMedical Device Manufacturing EngineerQuality Assurance Engineer
CredentialsBachelor's in engineering or related field; certifications like ASQ CQE beneficialBachelor's in engineering, quality assurance, or related; certifications like ASQ CQE or CQA common
Work EnvironmentManufacturing plants, production lines, R&D labsQuality labs, manufacturing sites, regulatory agencies
Industry UsageDesign, develop, and optimize manufacturing processesEnsure product quality, compliance, and process improvements

While both roles work within the medical device industry and require similar credentials, the Medical Device Manufacturing Engineer focuses on manufacturing processes and product development, whereas the Quality Assurance Engineer emphasizes maintaining quality standards and regulatory compliance.

What are popular job titles related to Medical Device Manufacturing Engineer jobs in Arizona?

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

Infographic showing various Medical Device Manufacturing Engineer 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, with an average salary of $79,782 per year, or $38.4 per hour.

Director Medical Device Manufacturing Operations

Castle Biosciences

Phoenix, AZ • On-site

Full-time

Medical, Retirement, PTO

This job post has expired today. Applications are no longer accepted.


Job description

Learn more at
Castle Biosciences Inc. is growing, and we are looking to hire a full-time Director Medical Device Manufacturing Operations working from our Phoenix, AZ office location, with a start date on or before October 1, 2026.
Why Castle Biosciences?
Exceptional Benefits Package:
  • Excellent Annual Salary + 35% 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 the Director Medical Device Manufacturing Operations
We're building a brand-new medical device manufacturing operation and need an experienced leader to build it from the ground up. This Director-level role will own everything from facility startup and process validation, to team building and day-to-day operations. All within an FDA-regulated environment. It's a high-visibility opportunity for someone who thrives on creating something from scratch and wants to make a real impact at a growing diagnostics company. What you'll do: Lead the startup and commercial launch of Castle's new manufacturing facility; from equipment installation and process validation through first production runs; build and lead the manufacturing team, including hiring managers, supervisors, and technicians, and establishing the training and operational systems they need to succeed; own day-to-day manufacturing performance including safety, quality, delivery, and cost; while driving continuous improvement and ensuring ongoing FDA/ISO compliance.
REQUIREMENTS
  • Bachelor's degree in Engineering, Life Sciences, Operations Management, or related field; advanced degree (MBA, MS Engineering, or related) preferred
  • 10+ years of progressive manufacturing leadership experience in medical device, diagnostics, or biotechnology industries, with at least 5 years in director-level or equivalent roles
  • Proven experience leading manufacturing startup operations, greenfield site launches, or significant facility expansions in FDA-regulated environments (21 CFR 820, ISO 13485, GMP)
  • Strong understanding of process validation (IQ/OQ/PQ), equipment qualification, and manufacturing documentation systems

*Please see the full job description at the end of the job ad.
SCHEDULE
  • This is a full-time onsite role in Phoenix, Monday-Friday, with hours that vary based on operational needs, especially during the startup phase.

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