Principal Software Quality Engineer

Posted 13 Days Ago
Be an Early Applicant
Mountain View, CA
In-Office
124K-165K Annually
Senior level
Healthtech
The Role
The Principal Software Quality Engineer will ensure software quality compliance throughout the product development lifecycle, support risk management activities, and oversee adherence to regulatory standards in medical software development.
Summary Generated by Built In

Based in Mountain View, CA., NeuroPace is a commercial-stage medical device company focused on transforming the lives of people suffering from epilepsy by reducing or eliminating the occurrence of debilitating seizures. Its novel and differential RNS System is the first and only commercially available, brain-responsive platform that delivers personalized, real-time treatment at the seizure source.

At NeuroPace, employees are our greatest asset. We are continually searching for solution-oriented individuals who can bring energy and creativity to our growing workforce. At NeuroPace, our success depends upon our ability to recruit and retain the most talented, enthusiastic and dedicated people we can find and providing them with a dynamic and challenging environment in which to thrive.

We are currently seeking a Principal Software Quality Engineer to join our team. This will be an individual contributor role working collaboratively with the Quality Design Assurance Engineering team, Product Development, Product MonitoringIT and Clinical Research teams on product design development through the product development lifecycle

Key Responsibilities

  • Participate in project teams and provide guidance to the team on software quality related activities (product software and firmware) assuring adherence to the software development lifecycle which may include PCCP strategy development. Assure that design controls are met; project plans include relevant software deliverables, and objective, measurable and verifiable customer and product requirements are established. Support establishment and adherence of project schedules. 
  • Update processes, implement templates, and mentor users in ensuring compliance with FDA QSR Part 820, ISO 13485ISO 62304 and ISO 62366. 
  • Ensure compliance with software risk standards by participating in risk management activities and ensuring compliance with risk management documentation, such as software risk analyses, safety analyses, communication analyses, sFMEA. 
  • Ensure compliance with cybersecurity procedures and standards. Ensure that software risk analyses include cybersecurity risks and define processes for threat modeling. Assist in the writing of cybersecurity risk management reports. 
  • Assess algorithmic design and implementation for robustness, bias, and adherence to regulatory requirements. Ensure proper validation and verification of AI-driven features, including transparency and explainability of models. 
  • Ensure compliance with SaMD regulatory landscape. 
  • Assure that software architecture is properly established and challenge software architectures/ designs and requirements for adequacy, safety, and robustness. 
  • Review software verification plans, protocols and reports for compliance with procedures and regulations. 
  • Apply usability engineering knowledge during applicable analyses and reviews. 
  • Represent Quality on the Software Change Board (SCB). 
  • Verify and implement laptop and tablet PC replacements to support manufacturing. 
  • Assess data and analytics as needed. 
  • Support audits by global regulators to support ISO 13485, MDSAP, Health Canada and CE Mark audits. 

Requirements

  • BS degree in a recognized engineering discipline, preferably Software Engineering. 
  • 10 years’ minimum experience as a quality professional, in the medical device industry. 
  • Demonstrated working knowledge of FDA QSR, ISO 13485, ISO 62304, ISO 62366, MDSAP, and MDR. 
  • Excellent verbal and written skills, interpersonal skills. 
  • ASQ certifications desired, but not necessary. 

$124-$165K Base - Compensation will be determined based on several factors, including but not limited to skill set, years of experience and geographic location.

NeuroPace is proud to be an equal opportunity employer and values the contributions of our culturally diverse workforce.

Fraud Alert: We're aware of fake job postings using NeuroPace's name. Legitimate communications only come from @neuropace.com emails and never request personal financial info or other personal data upfront. Please verify suspicious messages by contacting us directly. View our current job openings: https://www.neuropace.com/about-neuropace/neuropace-careers/


Benefits

  • Medical, Dental & Vision Insurance
  • Voluntary Life
  • 401K
  • RSU
  • 529 plan
  • ESPP Program
  • Health & Wellness Program
  • Generous Paid Time Off plus eleven paid holidays
  • FSA & Commuter Benefits

NeuroPace is proud to be an equal opportunity employer and values the contributions of our culturally diverse workforce.

San Francisco and Los Angeles applicants: The Company will consider for employment qualified applicants with Criminal Histories in a manner consistent with the requirements of the Los Angeles Fair Chance in Hiring Ordinance or the San Francisco Fair Chance Ordinance (as applicable)

PRIVACY NOTICE:  NeuroPace takes its responsibility to protect your personal information seriously, and it uses reasonable safeguards to avoid unauthorized use or disclosure of it, and inadvertent loss or impermissible alteration of it.  NeuroPace complies with all applicable federal and state laws and regulations that govern the handling of your personal information.  If you would like more detailed information on NeuroPace’s privacy policies, please refer to neuropace.com/privacy/ for reference.  NeuroPace retains candidate resumes and applications in its files for future reference and/or consideration for other available job postings.  If you do not wish for your resume and applications materials to be retained in NeuroPace files, or wish to obtain a listing of any personal information that NeuroPace has stored about you, please contact us at [email protected]



Top Skills

Ai Algorithms
Cybersecurity
Fda Qsr
Iso 13485
Iso 62304
Iso 62366
Usability Engineering
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The Company
HQ: Mountain View, CA
198 Employees
Year Founded: 1999

What We Do

The RNS® System is an award-winning technology developed and manufactured in Silicon Valley that has been recognized for its innovation. Similar to a pacemaker that monitors and responds to heart rhythms, the RNS System is the world's first and only medical device that can monitor and respond to brain activity.

NeuroPace was founded to design, develop, manufacture and market implantable devices for the treatment of neurological disorders with responsive stimulation. The company's initial focus is the treatment of epilepsy, a debilitating neurological disorder affecting approximately 1% of the population worldwide.In addition to treating epilepsy, responsive neurostimulation holds the promise of treating several other disabling medical disorders that impact the quality of life for millions of patients around the world.

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