Principal Software Quality Engineer

Who you are

You have extensive experience in software quality engineering, particularly in the medical device industry, where you understand the critical importance of compliance and quality assurance in product development. You are detail-oriented and have a strong grasp of software development lifecycles, ensuring that all design controls are met and that customer requirements are clearly defined and verifiable. Your collaborative spirit allows you to work effectively with cross-functional teams, including Product Development and Clinical Research, to drive quality initiatives.

You possess a proactive mindset, always looking for ways to improve processes and ensure that quality is embedded in every stage of product development. Your ability to communicate complex quality concepts to non-technical stakeholders is a key strength, enabling you to advocate for best practices in software quality assurance. You are committed to continuous learning and staying updated with the latest industry standards and technologies.

Desirable

Experience with regulatory standards specific to medical devices, such as ISO 13485 or FDA regulations, would be a significant advantage. Familiarity with automated testing tools and methodologies can enhance your contributions to the team. A background in firmware quality assurance is also beneficial, as it complements your software quality expertise.

What you'll do

In this role, you will participate in project teams, providing guidance on software quality-related activities throughout the product development lifecycle. You will ensure that all software deliverables meet the established quality standards and that project plans incorporate relevant quality assurance activities. Your responsibilities will include developing and implementing quality control strategies, conducting audits, and facilitating training sessions for team members on quality assurance best practices.

You will work closely with the Quality Design Assurance Engineering team to establish and maintain design controls, ensuring that all software and firmware meet regulatory requirements. Your role will involve reviewing project plans and deliverables, providing feedback, and ensuring that customer and product requirements are objective, measurable, and verifiable.

Collaboration is key in this position, as you will engage with various teams, including IT and Clinical Research, to align quality assurance efforts with overall product goals. You will also be responsible for documenting quality assurance processes and results, contributing to the continuous improvement of the quality management system.

What we offer

At NeuroPace, we value our employees as our greatest asset and strive to create a supportive and challenging work environment. You will have the opportunity to work on innovative medical technologies that have a direct impact on the lives of individuals suffering from epilepsy. We offer competitive compensation and benefits, along with opportunities for professional growth and development within the company. Join us in our mission to transform lives through cutting-edge medical devices.