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Medical Device Staff Engineer Jobs (NOW HIRING)

Staff Engineer - Medical Device

Brea, CA · On-site

$115K - $160K/yr

Trains office, field, and/or laboratory staff and entry level engineers. Provides technical ... This position also provides health benefits such as medical, dental and vision; wellness benefits ...

Staff Engineer - Medical Device

Brea, CA · Hybrid

$115K - $160K/yr

... medical technology. * University Degree in Electrical Engineering or related field. * 10+ years of ... Trains office, field, and/or laboratory staff and entry level engineers. Provides technical ...

Staff Engineer - Medical Device

Brea, CA · Hybrid

$115K - $160K/yr

... medical technology. * University Degree in Electrical Engineering or related field. * 10+ years of ... Trains office, field, and/or laboratory staff and entry level engineers. Provides technical ...

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Medical Device Assembler

Temecula, CA · On-site

$19.25 - $23.33/hr

Medical Device Assembler Location: Temecula, CA Employment Type: Full-Time / Contract Pay Rate: $19 ... tier consulting and staffing solutions across industries like technology, engineering ...

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Medical Device Assembler

Temecula, CA · On-site

$19.25 - $23.33/hr

Medical Device Assembler Location: Temecula, CA Employment Type: Full-Time / Contract Pay Rate: $19 ... tier consulting and staffing solutions across industries like technology, engineering ...

Medical Device Assembler

Temecula, CA · On-site

$19.25 - $23.33/hr

Medical Device Assembler Location: Temecula, CA Employment Type: Full-Time / Contract Pay Rate: $19 ... tier consulting and staffing solutions across industries like technology, engineering ...

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

Assemble medical devices and components according to engineering drawings, work instructions, and ... Prior experience in medical device assembly, electronics assembly, or precision manufacturing ...

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Medical Device Assembler

Temecula, CA · On-site

$19.25 - $23.33/hr

Medical Device Assembler Location: Temecula, CA Employment Type: Full-Time / Contract Pay Rate: $19 ... tier consulting and staffing solutions across industries like technology, engineering ...

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Medical Device Assembler

Temecula, CA · On-site

$19.25 - $23.33/hr

Medical Device Assembler Location: Temecula, CA Employment Type: Full-Time / Contract Pay Rate: $19 ... tier consulting and staffing solutions across industries like technology, engineering ...

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

Assemble medical devices and components according to engineering drawings, work instructions, and ... Prior experience in medical device assembly, electronics assembly, or precision manufacturing ...

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

Assemble medical devices and components according to engineering drawings, work instructions, and ... Prior experience in medical device assembly, electronics assembly, or precision manufacturing ...

Job Title: Medical Device Assembler Location: Madison, WI (Onsite) Pay Rate: $23-24/hr on W2 ... Engineering group as required. Working Conditions: Clean, temperature controlled environment.

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Showing results 1-20

Medical Device Staff Engineer information

See salary details

$23K

$99.3K

$192.5K

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

As of Sep 13, 2026, the average yearly pay for medical device staff engineer in the United States is $99,330.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,000.00 and $125,000.00 per year, depending on experience, location, and employer.

What is a medical device staff engineer?

Medical Device Staff Engineers are experienced professionals who design, develop, and oversee the production of medical devices. They ensure that devices meet regulatory standards, function safely, and address clinical needs. In addition to technical responsibilities, they often mentor junior engineers, lead project teams, and collaborate with cross-functional departments such as quality, manufacturing, and regulatory affairs. Their expertise is crucial in bringing innovative and compliant medical technologies to market.

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

To thrive as a Medical Device Staff Engineer, you need a solid background in biomedical, mechanical, or electrical engineering, often with a bachelor’s or master’s degree and relevant industry experience. Familiarity with CAD software, regulatory standards like FDA 21 CFR Part 820, and design control systems is commonly required. Strong problem-solving, project management, and cross-functional communication skills help you lead teams and navigate complex technical challenges. These capabilities ensure safe, compliant, and innovative medical device development in a highly regulated environment.

How do medical device staff engineers typically collaborate with cross-functional teams during product development?

Medical Device Staff Engineers frequently work alongside professionals from regulatory, quality assurance, manufacturing, and clinical teams throughout the product development lifecycle. They often serve as technical leaders, facilitating communication between design teams and other departments to ensure compliance with industry standards and successful project outcomes. This collaborative environment requires strong interpersonal skills and the ability to translate complex engineering requirements into actionable tasks for non-engineering colleagues. Additionally, they may lead or participate in design reviews, risk assessments, and troubleshooting sessions to address challenges as they arise.

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

AspectMedical Device Staff EngineerMedical Device Engineer
CredentialsBachelor's or Master's in Engineering, certifications like RAPS or ISO standardsBachelor's or Master's in Engineering, similar certifications
Work EnvironmentDesign, development, and testing in R&D or manufacturing settingsDesign, testing, and quality assurance in manufacturing or R&D
Industry UsageUsed across medical device companies for project leadershipCommonly used for core engineering roles in medical device firms

The Medical Device Staff Engineer typically holds a more senior or specialized role within the engineering team, often leading projects and providing technical expertise. In contrast, the Medical Device Engineer focuses on core engineering tasks such as design and testing. Both roles require similar credentials and work environments, but the Staff Engineer usually has greater responsibilities and experience.

What cities are hiring for Medical Device Staff Engineer jobs?

Cities with the most Medical Device Staff Engineer job openings:

What states have the most Medical Device Staff Engineer jobs?

States with the most job openings for Medical Device Staff Engineer jobs include:

What are popular job titles related to Medical Device Staff Engineer jobs?

For Medical Device Staff Engineer jobs, the most frequently searched job titles are:

Staff Engineer - Medical Device

Brea, CA • On-site

UL Solutions
Professional, Scientific, and Technical Services • 10K+ employees

$115K - $160K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 16 days ago


UL Solutions rating

8.4

Company rating: 8.4 out of 10

Based on 28 frontline employees who took The Breakroom Quiz


Job description


This is a hybrid role requiring 3 days onsite in Brea, CA.
Responsibilities
  • Represents UL on harmonized standards development committees.
  • Delivers technical training content to customers or at public events.
  • Independently determines project scope, develops a preliminary plan of investigation, and determines project specifications such as cost, time, and sample requirements by analyzing client input, available supplemental data, and product construction. Projects may include travel to conduct or witness tests at client sites.
  • Initiates communication with clients to promote and explain the benefits of new and existing services. Follows up on contacts from clients. Communicates with clients to discuss technical issues, explain UL procedures and requirements, convey project cost, and negotiate completion date and sample requirements. Acts to address client concerns and to resolve client issues. Provides technical assistance to clients in reference to product inspection and follow-up services.
  • Establishes appropriate test programs by reviewing files and manufacturer's information, examining samples, and applying UL requirements. Is familiar with applicable standards, company manuals and appropriate technical literature. Examines samples for compliance with UL requirements and notifies client of any areas in which the product is not in compliance or of any changes in project scope or specifications.
  • Coordinates complex laboratory activities by preparing data sheets and instructions to technicians, scheduling and reviewing work of laboratory technicians and engineering assistants and establishing completion dates. May sometimes conduct the testing. Coordinates administrative aspects of project management. May serve as Project Handler of record and/or Reviewer of record as assigned.
  • Communicates project status and results to clients through frequent contact and by preparing reports. Prepares Follow-Up Service Procedures and information pages.
  • Integrates continuous improvement concepts and techniques into all aspects of the job.
  • Resolves engineering issues associated with Variation Notices by analyzing and reporting on the acceptability of the variations.
  • Assists in the development of UL requirements. Assists in developing special test methods and test equipment. Analyzes test program for adequacy and sequence. May coordinate and/or perform File Reviews, as directed. May represent UL at industry related functions such as seminars and trade shows.
  • Provide complex sales support such as giving presentations during client visits.
  • Directs and reviews work of assigned staff. Trains office, field, and/or laboratory staff and entry level engineers. Provides technical assistance in several product categories, operations or systems to laboratory and/or field staff.
  • Performs quality systems and technical audits of customer laboratories.
  • Performs other duties as directed.

Qualifications
  • University Degree in Electrical Engineering or related field.
  • 10+ years of Compliance Engineering experience as Evaluator and Reviewer in the following core standards: IEC 60601-1, IEC 60601-1-6, IEC 60601-1-8, IEC 60601-1-11.
  • Additional experience as Evaluator and Reviewer in 60601 series particular standards, such as IEC 60601-2-2, IEC 60601-2-18, IEC 60601-2-47, ISO 80601-2-56, ISO 80601-2-61, ISO 80601-2-12, ISO 80601-2-74, IEC 60601-2-77, IEC 60601-2-78, IEC 60601-2-33, IEC 60601-2-37, IEC 60601-2-43, IEC 60601-2-44, IEC 60601-2-45, IEC 60601-2-37, IEC 60601-1-3.
  • Demonstrated ability to apply project-handling concepts in use in areas of expertise, including application to complex, new, or unusual products.
  • Strong communication skills and ability to interact and connect with customers.
  • Proven ability to be innovative and creative.
  • Desire to work within a team environment.
  • Comfortable in laboratory environments performing hands-on engineering.
  • Excellent interpersonal skills.
  • Able to provide unique solutions to complex problems.

What we offer:
  • Total Rewards: We understand compensation is an important factor as you consider the next step in your career. The estimated salary range for this position is $115,000-160,000 and is based on multiple factors, including job-related knowledge/skills, experience, geographical location, as well as other factors. This position is eligible for annual bonus compensation with a target payout of 20% of the base salary. This position also provides health benefits such as medical, dental and vision; wellness benefits such as mental and financial health; and retirement savings (401K) commensurate with the standard rewards offered in each individual location or country. We also provide full-time employees with paid time off including vacation (15 days), holiday including floating holidays (12 days) and sick time off (72 hours).

Learn More:
Curious? To learn more about us and the work we do, visit our company page www.UL.com
#LI-EH1
#LI-Hybrid
About Us
A global leader in applied safety science, UL Solutions (NYSE: ULS) transforms safety, security and sustainability challenges into opportunities for customers in more than 110 countries. UL Solutions delivers testing, inspection and certification services, together with software products and advisory offerings, that support our customers' product innovation and business growth. The UL Mark serves as a recognized symbol of trust in our customers' products and reflects an unwavering commitment to advancing our safety mission. We help our customers innovate, launch new products and services, navigate global markets and complex supply chains, and grow sustainably and responsibly into the future. Our science is your advantage.
About the Team
Every product needs to be safe. But for medical devices, it's absolutely essential. For manufacturers, getting medical devices approved can be incredibly complex. That's where our team of experts comes in. Together, we help improve medical outcomes. We test, advise and use our world-class knowledge to help manufacturers navigate changing standards and regulations, so they can provide people around the world with innovative products that save and improve lives. Whether it's equipment to help someone walk again or an incubator for a premature baby, our experts are behind them all, helping to ensure their safety. Join our team, connect with global experts and help shape the next generation of medical technology.

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