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60601 Jobs in Kansas (NOW HIRING)

Engenious Design

Systems Engineer

Prairie Village, KS · On-site

Experience interpreting and applying medical device standards such as ISO 60601-1, ISO 13485 etc., or similar experience in a regulated industry Nice to haves: * Experience leading cross-functional ...

Engenious Design

Systems Engineer

Prairie Village, KS · On-site

Experience interpreting and applying medical device standards such as ISO 60601-1, ISO 13485 etc., or similar experience in a regulated industry Nice to haves: * Experience leading cross-functional ...

Engenio

Human Factors Engineer

Prairie Village, KS · On-site

$80 - $100/hr

Be a subject‑matter expert in relevant standards documentation including but not limited to IEC 60601, IEC 62366, ISO 14971, and AAMI/ANSI HE75. * Prepare thorough documentation for regulatory ...

Proven

Senior Mechanical Engineer

Olathe, KS · On-site

$98K - $130K/yr

Ability to interpret and design for compliance with medical / mechanical safety standards (IEC 60601-1). * Ability to conduct biocompatibility analyses and design for compliance with ISO 10993-1 ...

Proven

Senior Mechanical Engineer

Olathe, KS · On-site

$150 - $200/hr

Ability to interpret and design for compliance with medical / mechanical safety standards (IEC 60601-1). * Ability to conduct biocompatibility analyses and design for compliance with ISO 10993-1 ...

Proven

Senior Mechanical Engineer

Olathe, KS · On-site

$98K - $130K/yr

Ability to interpret and design for compliance with medical / mechanical safety standards (IEC 60601-1). * Ability to conduct biocompatibility analyses and design for compliance with ISO 10993-1 ...

Vantage MedTech

Senior Mechanical Engineer

Olathe, KS · On-site

$100 - $125/hr

Ability to interpret and design for compliance with medical / mechanical safety standards (IEC 60601-1). * Ability to conduct biocompatibility analyses and design for compliance with ISO 10993-1 ...

Vantage MedTech

Senior Mechanical Engineer

Olathe, KS · On-site

$101K - $133K/yr

Ability to interpret and design for compliance with medical / mechanical safety standards (IEC 60601-1). * Ability to conduct biocompatibility analyses and design for compliance with ISO 10993-1 ...

All Jobs60601 Jobs60601 Jobs in Kansas

60601 information

See Kansas salary details

$4

$40

$61

How much do 60601 jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for 60601 in Kansas is $40.29, according to ZipRecruiter salary data. Most workers in this role earn between $32.69 and $48.18 per hour, depending on experience, location, and employer.

What are 60601 standards?

The 60601 standards refer to the IEC 60601 series, which are international standards for the safety and performance of medical electrical equipment. These standards ensure that medical devices meet essential requirements for safety, reliability, and electromagnetic compatibility. Compliance with IEC 60601 is often required for medical devices to be marketed and used in hospitals and healthcare settings. The standards cover various aspects, including basic safety, essential performance, and specific requirements for different types of medical equipment.

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

To thrive as a Medical Device Quality Engineer specializing in IEC 60601 compliance, you need a solid background in biomedical engineering or a related field, along with knowledge of regulatory standards for medical electrical equipment. Familiarity with compliance testing tools, risk management software, and quality systems such as ISO 13485 is typically required. Strong attention to detail, analytical thinking, and effective communication are essential soft skills for ensuring product safety and collaborating across teams. These abilities are crucial for maintaining regulatory compliance and ensuring the safety and effectiveness of medical devices in the healthcare industry.

What are common challenges faced by professionals working with IEC 60601 compliance, and how can they be addressed?

Professionals involved in IEC 60601 compliance often face challenges such as staying up-to-date with evolving standards, ensuring thorough documentation, and coordinating across departments like engineering and regulatory affairs. Addressing these challenges typically involves ongoing training, implementing robust project management tools, and fostering open communication among cross-functional teams. Regular internal audits and collaboration with external testing labs can also help ensure compliance and reduce the risk of costly redesigns or certification delays.

What is the difference between 60601 vs Medical Equipment Technician?

Aspect60601Medical Equipment Technician
CertificationsOften requires compliance with IEC 60601 standards, but not a specific certificationTypically requires certification in medical equipment repair or biomedical technology
Work EnvironmentHospitals, clinics, medical device manufacturingMedical facilities, repair shops, biomedical departments
Industry UsageStandards for medical electrical equipment safetyMaintains and repairs medical devices

While 60601 refers to safety standards for medical electrical equipment, Medical Equipment Technicians focus on repairing and maintaining such devices. Understanding 60601 is essential for technicians to ensure compliance and safety in their work.

60601 jobs near you
Infographic showing various 60601 job openings in Kansas as of July 2026, with employment types broken down into 96% Full Time, 1% Part Time, and 3% Contract. Highlights an 95% Physical, 4% Hybrid, and 1% Remote job distribution, with an average salary of $83,800 per year, or $40.3 per hour.

Systems Engineer

Prairie Village, KS • On-site

Engenious Design
Medical Equipment and Supplies Manufacturing • 11 - 50 employees
Learn more about Engenious Designexternal

Full-time

Re-posted 25 days ago

Job description

We’re seeking an experienced product development Systems Engineer who can think big-picture while staying hands-on across diverse technologies. You’ll define user needs, drive system‑level requirements, and unite electrical, mechanical, and software disciplines into cohesive products. Acting as the connective tissue across designers, engineers, and clients, you’ll navigate tradeoffs, manage risk, and tackle complex integration challenges to deliver life‑changing medical and high‑tech products.
What You’ll Do:
  • Maintain the System View: Act as the holistic thinker for the product—maintaining a clear mental model of the system, identifying roadblocks early, and guide the team toward effective solutions.
  • Lead Cross-Functional Integration: Coordinate electrical, mechanical, software, industrial design, and test workstreams to ensure the product functions as a cohesive system.
  • Drive Requirements & Traceability: Lead the definition of user needs and product requirements, maintaining clear traceability from requirements to design decisions, risk management, and verification.
  • Own Risk Management: Proactively identify, prioritize, document, and manage technical and program risks, working closely with the design team to develop and execute mitigation strategies.
  • Act as a Technical Investigator: Use prototypes, proof-of-concept builds, and engineering testing to validate concepts and inform design direction.
  • Enable Informed Decisions: Communicate system architecture, progress, risks, and tradeoffs clearly to teams and clients, empowering confident design decisions.
  • Guide Compliance & Documentation: Ensure development follows the governing QMS and regulatory standards while maintaining a right-sized Design Development File.

Position Details:
This is a full-time, permanent position. This leadership position is based in our Kansas City design center, and not available as a remote job.
Qualifications:
  • 5+ years of applicable experience in electromechanical/embedded system product development
  • Degree in a relevant engineering background (e.g Biomedical, Mechanical, Electrical, Software), or equivalant experience.
  • Experience interpreting and applying medical device standards such as ISO 60601-1, ISO 13485 etc., or similar experience in a regulated industry
Nice to haves:
  • Experience leading cross-functional teams of engineers and designers

While we recognize that top talent comes from all over the world, we are a small team and are not able to offer visa sponsorship at this time. Candidates must be authorized to work in the United States without requiring visa sponsorship

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