We are testing titling to see which attracts the most qualified candidates. Please only apply to ... regulated medical device software. These systems will support the full software lifecycle, from ...
We are testing titling to see which attracts the most qualified candidates. Please only apply to ... regulated medical device software. These systems will support the full software lifecycle, from ...
... medical device requirements. * Contribute to usability requirements, use scenarios, risk identification, and mitigation strategies. * Support formative and summative usability testing initiatives.
... medical device requirements. * Contribute to usability requirements, use scenarios, risk identification, and mitigation strategies. * Support formative and summative usability testing initiatives.
Senior User Experience Designer
Austin, TX · On-site
... medical device requirements. * Contribute to usability requirements, use scenarios, risk identification, and mitigation strategies. * Support formative and summative usability testing initiatives.
Senior User Experience Designer
Austin, TX · On-site
... medical device requirements. * Contribute to usability requirements, use scenarios, risk identification, and mitigation strategies. * Support formative and summative usability testing initiatives.
Sr Product Quality Engineer - Onsite
Austin, TX · On-site
$87K - $118K/yr
Proven experience working with and understanding Quality System requirements in the medical device ... testing, or otherwise participating in the employee selection process, please fill out the ...
Sr Product Quality Engineer - Onsite
Austin, TX · On-site
$87K - $118K/yr
Proven experience working with and understanding Quality System requirements in the medical device ... testing, or otherwise participating in the employee selection process, please fill out the ...
... medical device manufacturing environment. This position provides advanced hands-on support for Coordinate Measuring Machines (CMMs), X-ray inspection systems, dye penetrant testing equipment ...
... medical device manufacturing environment. This position provides advanced hands-on support for Coordinate Measuring Machines (CMMs), X-ray inspection systems, dye penetrant testing equipment ...
... medical device manufacturing environment. This position provides advanced hands-on support for Coordinate Measuring Machines (CMMs), X-ray inspection systems, dye penetrant testing equipment ...
... medical device manufacturing environment. This position provides advanced hands-on support for Coordinate Measuring Machines (CMMs), X-ray inspection systems, dye penetrant testing equipment ...
Be Seen First
Design Verification Engineer - Design Assurance
Austin, TX · On-site
$38 - $42/hr
... testing, so this person will support multiple concurrent workstreams. The ideal candidate is ... relevant medical device design verification or design assurance experience * Strong technical ...
Quick apply
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Design Verification Engineer - Design Assurance
Austin, TX · On-site
$38 - $42/hr
... testing, so this person will support multiple concurrent workstreams. The ideal candidate is ... relevant medical device design verification or design assurance experience * Strong technical ...
Be Seen First
Design Verification Engineer - Design Assurance
Austin, TX · On-site
$38 - $42/hr
... testing, so this person will support multiple concurrent workstreams. The ideal candidate is ... relevant medical device design verification or design assurance experience * Strong technical ...
Quick apply
Be Seen First
Design Verification Engineer - Design Assurance
Austin, TX · On-site
$38 - $42/hr
... testing, so this person will support multiple concurrent workstreams. The ideal candidate is ... relevant medical device design verification or design assurance experience * Strong technical ...
Hands-on experience with prototyping, testing, and lab operations Preferred Qualifications: * Knowledge of regulatory standards relevant to medical device development * Experience with inventory ...
Hands-on experience with prototyping, testing, and lab operations Preferred Qualifications: * Knowledge of regulatory standards relevant to medical device development * Experience with inventory ...
Sr. Quality Engineer
Austin, TX · On-site
$87K - $118K/yr
Knowledge and experience with software as a medical device. * Independently plan, develop, maintain ... Perform complex testing activities involving multi-system integrations, data interfaces ...
Sr. Quality Engineer
Austin, TX · On-site
$87K - $118K/yr
Knowledge and experience with software as a medical device. * Independently plan, develop, maintain ... Perform complex testing activities involving multi-system integrations, data interfaces ...
Sr. Quality Engineer
Austin, TX · On-site
$87K - $118K/yr
Knowledge and experience with software as a medical device. * Independently plan, develop,maintain ... Perform complex testing activities involving multi-system integrations, data interfaces ...
Sr. Quality Engineer
Austin, TX · On-site
$87K - $118K/yr
Knowledge and experience with software as a medical device. * Independently plan, develop,maintain ... Perform complex testing activities involving multi-system integrations, data interfaces ...
Systems Integration & Controls Engineer
Austin, TX · On-site
$165K/yr
... and testing device. This device bridges the gap between physical hardware, biology, and data ... medical device or IVD software design controls (IEC 62304 / ISO 14971). * Experience establishing ...
Systems Integration & Controls Engineer
Austin, TX · On-site
$165K/yr
... and testing device. This device bridges the gap between physical hardware, biology, and data ... medical device or IVD software design controls (IEC 62304 / ISO 14971). * Experience establishing ...
Systems Integration & Controls Engineer
Austin, TX · On-site
$95K/yr
... and testing device. This device bridges the gap between physical hardware, biology, and data ... medical device or IVD software design controls (IEC 62304 / ISO 14971). * Experience establishing ...
Systems Integration & Controls Engineer
Austin, TX · On-site
$95K/yr
... and testing device. This device bridges the gap between physical hardware, biology, and data ... medical device or IVD software design controls (IEC 62304 / ISO 14971). * Experience establishing ...
Automated Inspection Quality Engineer
Austin, TX · On-site
$71K - $92K/yr
... biomedical, medical device field) with an in-depth knowledge of current Good Manufacturing ... testing, processing, storing, and distribution of raw materials, components, and tissues/products.
Automated Inspection Quality Engineer
Austin, TX · On-site
$71K - $92K/yr
... biomedical, medical device field) with an in-depth knowledge of current Good Manufacturing ... testing, processing, storing, and distribution of raw materials, components, and tissues/products.
Automated Inspection Quality Engineer
$72K - $93K/yr
... biomedical, medical device field) with an in-depth knowledge of current Good Manufacturing ... testing, processing, storing, and distribution of raw materials, components, and tissues/products.
Automated Inspection Quality Engineer
$72K - $93K/yr
... biomedical, medical device field) with an in-depth knowledge of current Good Manufacturing ... testing, processing, storing, and distribution of raw materials, components, and tissues/products.
... and testing device. This device bridges the gap between physical hardware, biology, and data ... medical device or IVD software design controls (IEC 62304 / ISO 14971). * Experience establishing ...
Quick apply
... and testing device. This device bridges the gap between physical hardware, biology, and data ... medical device or IVD software design controls (IEC 62304 / ISO 14971). * Experience establishing ...
Participate in rigorous testing and code reviews * Create design documents & follow regulatory procedures and guidelines What Makes You Stand Out * * Experience in the Medical Device industry
Participate in rigorous testing and code reviews * Create design documents & follow regulatory procedures and guidelines What Makes You Stand Out * * Experience in the Medical Device industry
The Brain Interfaces Team is responsible for the design, manufacturing, and testing of all systems ... Knowledge of regulatory standards relevant to medical device development * Experience with ...
The Brain Interfaces Team is responsible for the design, manufacturing, and testing of all systems ... Knowledge of regulatory standards relevant to medical device development * Experience with ...
The Brain Interfaces Team is responsible for the design, manufacturing, and testing of all systems ... Knowledge of regulatory standards relevant to medical device development * Experience with ...
The Brain Interfaces Team is responsible for the design, manufacturing, and testing of all systems ... Knowledge of regulatory standards relevant to medical device development * Experience with ...
Neurodiagnostic EEG Technology Network Specialist
Austin, TX · On-site
$44.99/hr
Deployment of integrated medical device ecosystems (Nihon Kohden system upgrades, Radman, Citrix ... acceptance testing, validation, and commissioning of complex systems, and provide technical ...
Neurodiagnostic EEG Technology Network Specialist
Austin, TX · On-site
$44.99/hr
Deployment of integrated medical device ecosystems (Nihon Kohden system upgrades, Radman, Citrix ... acceptance testing, validation, and commissioning of complex systems, and provide technical ...
Medical Device Testing information
See Austin, TX salary details
$23.55 is the 25th percentile. Wages below this are outliers.
$21.21 - $25.65
47% of jobs
The median wage is $26.88 / hr.
$25.65 - $30.09
9% of jobs
$30.09 - $34.53
0% of jobs
$34.53 - $38.97
4% of jobs
$42.65 is the 75th percentile. Wages above this are outliers.
$38.97 - $43.41
17% of jobs
$43.41 - $47.85
8% of jobs
$47.85 - $52.29
7% of jobs
$52.29 - $56.73
4% of jobs
$56.73 - $61.17
0% of jobs
$61.17 - $65.61
0% of jobs
$65.61 - $70.05
2% of jobs
$21
$36
$70
How much do medical device testing jobs pay per hour?
What are the key skills and qualifications needed for medical device testing?
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.
What does medical device testing involve?
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 medical device testing?
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.
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Job description
Team Description:
Join the Quality Systems Team, where our mission is to ensure compliance with applicable regulatory standards by designing scalable, efficient, and automation-driven systems. We focus on embedding compliance directly into engineering workflows rather than treating it as a manual or reactive function.
We are a team of industry-experienced professionals who apply systems thinking and creative problem-solving to build a durable compliance infrastructure that supports rapid development. Our vision is to establish internal design and quality systems that exceed FDA expectations while enabling fast iteration and deployment of complex, safety-critical software products.
Job Description and Responsibilities:
Please note, this is a duplicate posting for the "Quality Systems Engineer" role. We are testing titling to see which attracts the most qualified candidates. Please only apply to one of the postings.Â
As a Software Design Controls Engineer, your primary responsibility will be to design, implement, and continuously improve software-focused design control systems with regulatory compliance embedded into their architecture.
You will build systems that eliminate ambiguity, reduce manual effort, and enable rapid and reliable development of regulated medical device software. These systems will support the full software lifecycle, from requirements definition through verification, validation, risk management, and release.
You will continuously optimize these systems to improve speed, traceability, and audit readiness while supporting aggressive development timelines and frequent design changes. Your responsibilities include, but are not limited to:
- Design and implement scalable software design controls systems aligned with IEC 62304 and FDA design control requirements (21 CFR 820.30)
- Develop and maintain end-to-end traceability frameworks linking:
- User needs
- Software requirements
- Risk controls
- Design outputs (code, architecture)
- Verification and validation evidence
- Integrate software risk management into design controls, ensuring alignment with ISO 14971 principles
- Build change control mechanisms capable of supporting:
- Rapid iteration
- Parallel development
- Same-day deployment
- Partner closely with software engineering teams to embed:
- Compliance with CI/CD pipelines
- Automated evidence generation
- Controlled release processes
- Own subsets of the Quality System related to software design controls, including but not limited to:
- Software Design Control processes
- Software Risk Management
- Software Change Control
- Software Verification & Validation traceability
Required Qualifications:Â
- Bachelor's degree in Electrical Engineering, Computer Science, or a related technical field
- Demonstrated experience designing or maintaining structured engineering or compliance systems
- Familiarity with software development lifecycles in regulated or safety-critical environments
- Working knowledge of:
- Design Controls
- Software requirements management
- Proficiency in basic scripting, automation, or querying (e.g., Python, SQL, or equivalent)
- Excellent written and verbal communication skills
- Strong problem-solving mindset with the ability to think in systems rather than silos
Preferred Qualifications:
- Familiarity with IEC 62304 (Medical Device Software Lifecycle Processes)
- Familiarity with FDA Design Controls (21 CFR 820.30)
- Familiarity with Design Risk Management (ISO 14971 principles)
- 1-3 years of experience in:
- Software Design Controls Engineer
- Software Quality
- Regulated software development
About NEURALINK
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
201 - 500 Employees
Headquarters location
San Francisco, CA, US
Year founded
2016