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How much do medical device testing jobs pay per hour?

As of Jun 11, 2026, the average hourly pay for medical device testing in Minnesota is $35.97, according to ZipRecruiter salary data. Most workers in this role earn between $24.23 and $44.95 per hour, depending on experience, location, and employer.

Does the medical device industry pay well?

Medical device testing professionals typically earn competitive salaries that vary based on experience, location, and certifications. Entry-level roles may start lower, but experienced testers with specialized skills can command higher wages, especially in regulated environments requiring knowledge of quality standards like ISO 13485.

What are the key skills and qualifications needed to thrive in the Medical Device Testing position, and why are they important?

To thrive in Medical Device Testing, you need a strong background in biomedical engineering, quality assurance, and regulatory compliance, often supported by a relevant degree. Hands-on experience with testing equipment, validation protocols, and familiarity with standards such as ISO 13485 and FDA guidelines are typically required. Attention to detail, analytical thinking, and clear documentation skills are essential soft skills for excelling in this field. These abilities ensure that devices meet safety and performance standards, protecting patient health and supporting company compliance.

Will AI replace medical device sales jobs?

AI is unlikely to fully replace medical device sales jobs, as these roles require relationship-building, product knowledge, and negotiation skills that are difficult for AI to replicate. Instead, AI can support sales professionals by providing data analysis, customer insights, and automating routine tasks. Success in this field often depends on interpersonal skills, technical understanding, and certifications, which remain essential despite technological advancements.

What is medical device testing?

Medical device testing involves evaluating medical equipment and devices to ensure they meet safety, performance, and regulatory standards. It includes procedures such as functional testing, durability testing, and compliance verification, often requiring knowledge of industry regulations and testing tools. Professionals in this field may work in controlled environments and need relevant certifications.

What are some typical daily responsibilities for someone working in Medical Device Testing?

Professionals in Medical Device Testing typically spend their days conducting tests on new or existing medical devices to ensure they meet quality, safety, and regulatory standards. This often involves following strict protocols, documenting results accurately, and troubleshooting any performance or compliance issues that arise. Team members frequently collaborate with engineers, regulatory specialists, and manufacturing staff to ensure seamless product development and problem resolution. There may also be tasks related to preparing reports for regulatory submissions or participating in audits. This role offers the opportunity to make a real impact on patient safety while working in a collaborative, fast-paced environment.

What is a Medical Device Testing job?

A Medical Device Testing job involves evaluating medical devices to ensure they meet regulatory standards, safety guidelines, and performance requirements. Professionals in this role conduct tests, analyze data, and document results to verify compliance with industry regulations such as FDA, ISO, and IEC standards. They work with engineers and regulatory teams to identify design flaws, improve product safety, and ensure reliability before market release. This job is crucial for preventing defects that could impact patient health and safety.

Are there any legit product testing jobs?

Medical device testing jobs are legitimate roles that involve evaluating the safety, functionality, and compliance of medical devices. These positions often require knowledge of industry standards, attention to detail, and sometimes certifications or training in quality assurance or regulatory requirements.
What are the most commonly searched types of Medical Device Testing jobs in Minnesota? The most popular types of Medical Device Testing jobs in Minnesota are:
What are popular job titles related to Medical Device Testing jobs in Minnesota? For Medical Device Testing jobs in Minnesota, the most frequently searched job titles are:
What job categories do people searching Medical Device Testing jobs in Minnesota look for? The top searched job categories for Medical Device Testing jobs in Minnesota are:
What cities in Minnesota are hiring for Medical Device Testing jobs? Cities in Minnesota with the most Medical Device Testing job openings:
Medical Device Testing jobs near you

Principal Firmware Engineer - Implantable Medical Devices

Enterra Medical, Inc.

Minneapolis, MN • On-site

$130K - $160K/yr

Full-time

Posted 12 days ago

Job description


Location: Minneapolis, MN Hybrid (In office weekly as needed)
Company Summary:
Enterra Medical is a medical device company dedicated to a singular focus: helping more people with chronic gastroparesis live better lives by advancing technology, expanding clinical science, and accelerating access to the Enterra® Therapy.
Position Overview
We are seeking a skilled Principal Firmware Engineer with specialized experience in developing firmware for active implantable medical devices. This role involves designing, developing, testing, and optimizing embedded software to ensure the safety, reliability, and performance of cutting-edge medical technologies. The ideal candidate will have a strong background in embedded systems, real-time operating systems, and regulatory compliance for medical devices.
Key Responsibilities
  • Design, develop, and test firmware for active implantable medical devices, ensuring high reliability and performance under strict power and size constraints.
  • Collaborate with cross-functional teams, including hardware engineers, software developers, and regulatory specialists, to integrate firmware with device hardware and external systems.
  • Implement and validate communication protocols (e.g., Bluetooth Low Energy, proprietary RF) for secure data transmission between active implantable devices and external interfaces.
  • Ensure compliance with medical device standards, such as ISO 13485, IEC 62304, and FDA regulations, throughout the development lifecycle.
  • Optimize firmware for low-power operation to extend the lifespan of active implantable devices.
  • Conduct risk analysis, debugging, and verification to ensure firmware meets safety and efficacy requirements.
  • Document all development processes, including design specifications, test plans, and validation reports, in accordance with regulatory requirements.
  • Support clinical trials and post-market surveillance by analyzing device performance and implementing firmware updates as needed.
Qualifications
  • Education: Bachelor’s or master’s degree in electrical engineering, Computer Engineering, Computer Science, or a related field.
  • Experience:
    • 7+ years of experience developing firmware for embedded systems, with at least 5 years focused on active implantable medical devices required.
    • Proven expertise in programming in C/C++ for resource-constrained environments required.
    • Experience with real-time operating systems (RTOS) and bare-metal programming.
    • Familiarity with medical device regulations (e.g., FDA, ISO 13485, IEC 62304).
    • Hands-on experience with low-power wireless communication protocols (e.g., BLE, Zigbee).
    • Experience using software development tools such as GitHub and Jira.
    • Experience conducting static analysis and unit testing using tools such as PC-Lint and GTest.
  • Skills:
    • Strong understanding of embedded systems architecture and hardware-software integration required.
    • Proficiency in debugging tools (e.g., JTAG, oscilloscopes, logic analyzers).
    • Knowledge of cybersecurity principles for medical devices, including encryption and secure data transfer.
    • Ability to work in a highly regulated environment with a focus on safety and quality.
    • Excellent problem-solving skills and attention to detail.
  • Preferred:
    • Knowledge of battery management systems for implantable devices.
    • Familiarity with Agile development methodologies.

Salary: $130,000-160,000 DOE
 

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