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Iec 60601 Jobs (NOW HIRING)

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 ...

Staff Engineer - Medical Device

Brea, CA · Hybrid

$115K - $160K/yr

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 ...

Staff Engineer - Medical Device

Brea, CA · Hybrid

$115K - $160K/yr

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 ...

Staff Engineer - Medical Device

Brea, CA · On-site

$115K - $160K/yr

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 ...

Technical Lead - Electrical

Boston, MA

$173K - $181K/yr

The role involves ownership of IEC 60601-1 and IEC 60601-1-2 compliance activities, in-house test capability development, hardware design reviews, root-cause investigations, and external ...

IEC 60601-1, IEC 60601-1-6 + 62366, IEC 60601-1-8, IEC 60601-1-9, IEC 60601-1-11, IEC 62304, IEC 60601-2-25, IEC 60601-2-27, IEC 80601-2-30, IEC 60601-2-46, IEC 60601-2-49, IEC 60601-2-52, ISO 80601 ...

Lead execution of basic safety and electrical safety verification per IEC 60601-1 and associated particular and collateral standards. * Perform basic safety tests including dielectric strength/hi pot ...

Perform and support IEC 60601 electrical safety testing for medical device products * Execute and document: * Leakage current testing * Ground continuity testing * Hipot testing * Insulation ...

Perform and support IEC 60601 electrical safety testing for medical device products * Execute and document: * Leakage current testing * Ground continuity testing * Hipot testing * Insulation ...

Senior System Engineer

Sudbury, MA · On-site

$109K - $149K/yr

Drive compliance testing strategy and execution for IEC 60601-1 electrical safety and IEC 60601-1-2 EMC requirements; coordinate lab testing, pre-compliance, and corrective actions. Plan and execute ...

Coordinate and support electrical safety (IEC/UL 60601-1, IEC 60601-2-2, IEC 60601-2-18) and EMC (IEC60601-1-2) certification testing. * Perform design control functions to ensure compliance with FDA ...

Senior System Engineer

Sudbury, MA

$109K - $149K/yr

Drive compliance testing strategy and execution for IEC 60601-1 electrical safety and IEC 60601-1-2 EMC requirements; coordinate lab testing, pre-compliance, and corrective actions. Plan and execute ...

Coordinate and support electrical safety (IEC/UL 60601-1, IEC 60601-2-2, IEC 60601-2-18) and EMC (IEC60601-1-2) certification testing. * Perform design control functions to ensure compliance with FDA ...

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Iec 60601 information

What is IEC 60601?

IEC 60601 is an international series of technical standards for the safety and essential performance of medical electrical equipment. It ensures that medical devices are safe for both patients and operators by addressing electrical, mechanical, and functional safety. Compliance with IEC 60601 is mandatory in many countries for manufacturers who want to market their medical devices. The standard is regularly updated to reflect new technological advances and safety requirements.

What are some common challenges faced by professionals working with IEC 60601 compliance in medical device development?

Professionals working with IEC 60601 compliance often face challenges related to interpreting complex safety and performance requirements, as well as keeping up with frequent updates to the standard. Ensuring comprehensive documentation and rigorous testing to meet both basic and collateral standards can be time-consuming. Collaboration with cross-functional teams, such as regulatory, engineering, and quality assurance, is essential to address issues early and streamline the approval process. Additionally, adapting designs to accommodate evolving regional regulations can be a significant challenge.

What are the key skills and qualifications needed to thrive as a medical device compliance engineer (IEC 60601), and why are they important?

To excel as a Medical Device Compliance Engineer specializing in IEC 60601, a solid background in electrical engineering, regulatory standards, and risk management is required, often supported by a relevant engineering degree. Familiarity with IEC 60601-1 standards, test equipment, and compliance management software is essential for the role. Strong attention to detail, analytical thinking, and effective communication are soft skills that help navigate complex regulatory requirements and cross-functional collaboration. These competencies ensure medical devices are safe, effective, and meet global regulatory standards for patient safety.

What is the difference between Iec 60601 vs Medical Equipment Technician?

AspectIec 60601Medical Equipment Technician
CertificationsMay require IEC 60601 compliance knowledgeTypically certified in medical equipment repair and maintenance
Work EnvironmentDesign, testing, and compliance of medical electrical devicesRepair, calibrate, and maintain medical equipment in healthcare settings
Industry UsageStandards for medical electrical devicesHands-on technical support in hospitals and clinics

IEC 60601 is a standard ensuring safety and performance of medical electrical equipment, while a Medical Equipment Technician focuses on maintaining and repairing such devices. The technician applies IEC 60601 standards in their work but is primarily involved in practical device support rather than standard development or compliance testing.

More about Iec 60601 jobs

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What states have the most Iec 60601 jobs?

States with the most job openings for Iec 60601 jobs include:

Infographic showing various Iec 60601 job openings in the United States as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 90% In-person, and 10% Hybrid job distribution.

Staff Engineer - Medical Device

UL Solutions

Brea, CA • On-site

$115 - $160/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 24 days ago


UL Solutions rating

8.3

Company rating: 8.3 out of 10

Based on 27 frontline employees who took The Breakroom Quiz

28th of 120 rated laboratories


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 estimatedsalary 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 pagewww.UL.com

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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