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Neuro Medical Device Jobs (NOW HIRING)

Medical Murray

R&D Quality Engineer II

Barrington, IL · On-site

$85K - $105K/yr

Position Overview If you are passionate about medical device innovation and thrive in fast-paced ... cardiology, neurology, and urology -- directly contributing to products that improve patient ...

Noctrix Health

Quality Engineer I

Pleasanton, CA · On-site

$80K - $120K/yr

Noctrix Health is redefining the treatment of chronic neurological disorders with clinically validated therapeutic wearables. Our team of medical device specialists, neuroscientists, and consumer ...

Noctrix Health

Quality Engineer I

Pleasanton, CA

$80K - $120K/yr

Noctrix Health is redefining the treatment of chronic neurological disorders with clinically validated therapeutic wearables. Our team of medical device specialists, neuroscientists, and consumer ...

Accordance Search Group

We are a world class medical device company seeking a nurse with ICU or ED critical care experience ... "neuro ICU" OR "CAUTI"

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Neuro Medical Device information

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$49

$96

How much do neuro medical device jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for neuro medical device in the United States is $49.84, according to ZipRecruiter salary data. Most workers in this role earn between $35.10 and $59.62 per hour, depending on experience, location, and employer.

What is the difference between Neuro Medical Device vs Neurotechnologist?

AspectNeuro Medical DeviceNeurotechnologist
Required CredentialsBiomedical engineering, technical certificationsNeuroscience, radiologic technology certifications
Work EnvironmentManufacturing, R&D, clinical settingsHospitals, clinics, labs
Industry UsageDesign, testing, and maintenance of neuro medical devicesOperating neurodiagnostic equipment, patient testing

Neuro Medical Device professionals focus on designing, testing, and maintaining neuro-related medical devices, often working in R&D or manufacturing environments. Neurotechnologists operate diagnostic equipment in clinical settings, performing tests to assess neurological functions. While both roles require knowledge of neuroscience, their work environments and primary responsibilities differ significantly.

What are neuro medical devices?

Neuro medical devices are specialized instruments or implants designed to diagnose, monitor, or treat disorders of the nervous system, including the brain, spinal cord, and peripheral nerves. These devices can include deep brain stimulators, neuroprosthetics, neurostimulators, and diagnostic equipment like EEGs. They play a crucial role in treating conditions such as epilepsy, Parkinson's disease, chronic pain, and spinal cord injuries. Advances in technology have made these devices more effective, minimally invasive, and tailored to individual patient needs.

What are some common challenges faced by professionals working with neuro medical devices, and how can they be addressed?

Professionals working with neuro medical devices often encounter challenges such as staying updated with rapidly evolving technologies, ensuring strict compliance with regulatory standards, and effectively collaborating with multidisciplinary teams. To address these challenges, staying engaged with ongoing education, participating in industry conferences, and developing strong communication skills with clinicians, engineers, and regulatory experts are essential. Additionally, maintaining meticulous documentation and actively seeking feedback from end-users can help improve device safety and efficacy.

What are the key skills and qualifications needed to thrive as a Neuro Medical Device Specialist, and why are they important?

To thrive as a Neuro Medical Device Specialist, you need a solid background in biomedical engineering, neuroscience, or a related field, often supported by a relevant degree and industry certifications. Familiarity with neurostimulation devices, imaging systems, and regulatory compliance standards like FDA or CE marking is typically required. Exceptional problem-solving, communication, and training skills help you support clinicians and effectively convey technical information. These skills are crucial for ensuring patient safety, device efficacy, and successful collaboration between healthcare providers and manufacturers.
Infographic showing various Neuro Medical Device job openings in the United States as of June 2026, with employment types broken down into 2% As Needed, 97% Full Time, and 1% Part Time. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $103,662 per year, or $49.8 per hour.
QMS Supervisor - Medical Devices

QMS Supervisor - Medical Devices

Elliquence

Baldwin, NY • On-site

Full-time

Posted 10 days ago

Job description

Quality Management Systems Supervisor
Job Summary
The Quality Management Systems Supervisor will oversee the development, implementation, and maintenance of the organization’s Quality Management System (QMS) to ensure compliance with industry regulations and standards (ISO 9001, ISO 13485, AS9100). Reporting to the Director of Quality Affairs, this individual will drive continuous improvement, support in leading in internal/external audits, manage CAPA processes, and provide cross-functional training to enhance quality awareness. 
Key Responsibilities
  • Manage the QMS structure, ensuring all policies, procedures, and Work Instructions (SOPs) are compliant with regulatory requirements and align with company strategic goals.
  • With guidance from the Quality Affairs Director, lead both internal and external audits (customer, registrar, regulatory), coordinate audit finding responses, and verify the effectiveness of corrective actions.
  • Lead root cause analysis (RCA) for non-conformances, customer complaints, and deviations, implementing effective Corrective and Preventive Actions (CAPA).
  • Drive continuous improvement initiatives using lean methodologies, SPC (Statistical Process Control), and data analysis to enhance operational efficiency.
  • Manage the electronic Quality Management Systems (eQMS) and ensure Document Control processes are current, accurate, and compliant.
  • Confirms alignment of all Quality programs within the organization.
  • Monitor and ensure the organization’s commitment to quality meets or exceeds customer requirements and the relevant regulatory standards.
  • Develop, trend, and report key QMS performance metrics (KPIs) to senior management and provide solutions to guide data-driven decision-making.
  • Develop training materials and educate staff on QMS procedures, GMP (Good Manufacturing Practices), or regulatory compliance to cultivate a culture of quality. 
  • Consistently review SOP and other services to improve quality and contain costs.

Required Qualifications
  • Minimum of 5 years of experience in a leading role in Quality Management Systems or Quality Assurance in the medical device industry required (spine or neuro device companies a plus).
  • Bachelor’s degree in Engineering, Life Sciences, Biomedical Engineering, Quality Management, or a related field. Master’s degree will be considered for 1 year work experience in related QMS field in medical device industry (preferably spine or neuro).
  • Strong knowledge of ISO 9001, ISO 13485, or AS9100:2016 standards.
  • Leadership ability in root cause analysis tools, Failure Mode and Effects Analysis (FMEA), Statistical Process Control (SPC), and electronic QMS software.
  • Certified Internal Auditor (ISO 9001/13485) preferred. 
  • Lean Six Sigma Certifications preferred (Black Belt and/or Green Belt)
Required Skills & Competencies
  • Excellent written and verbal communication skills for interfacing customers and regulators.
  • Proven ability to partner and influence cross-functional teams, lead/mentor through collaboration and influence without direct authority.
  • Strong analytical abilities to interpret data and implement effective, sustainable solutions.
  • Proficient in problem solving with independent thought and judgement while using resources both internally and externally.
  • Work efficiently and proactively cross functionally in a team setting while being sensitive to deadlines.
  • High level of accuracy in document review and compliance assessment. 
  • Successful record of ability to work both independently and in a team environment.
  • Skilled in statistical quality methods, Lean principles, Six Sigma, and Root Cause Analysis for data-driven decision-making.
  • Determined and proactive mindset who is motivated to make a difference with a high standard of excellence.
Preferred Qualifications
  • ASQ Certified Quality Auditor (CQA) or Certified Quality Engineer (CQE).
  • Experience in a heavily regulated industry (Medical Device or Pharma).
  • Administration experience for document control.

Salary Range: 95,000-105,000/annual
 

An employment offer is based on the candidate's professional experience, specialty, skillset, education, geography, related licenses or certifications, and other business needs. The compensation range indicated does not include other forms of compensation or benefits.

We value the diversity of our team and inspire creativity in our innovation. elliquence proudly provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any kind without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state and local laws.

We are committed to working with and providing reasonable accommodation to individuals with disabilities. If you need any reasonable accommodation due to a disability for any part of the application process, please email hr@elliquence.com.


 

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