Quality Engineer II

Epia Neuro • Alameda, CA

6d • Hybrid

About The Position

Epia Neuro is a neural technology company developing intent-driven systems designed to restore function and independence for people living with neurological conditions. Its platform integrates implantable neural interfaces, adaptive algorithms, and assistive devices to translate neural intent into real-world action. The company’s initial focus is stroke-related motor impairment, with expansion in cognitive decline and other neurological disorders, focusing on long-term solutions for the growing aging population. The Role We're looking for a Quality Engineer II who will bring rigor, flexibility, and a collaborative mindset to our Quality function. Reporting to the Quality Manager, you will own several operational pillars of our Quality Management System, helping the team move faster without sacrificing rigor or compliance. This is a great fit for someone with a few years of Quality or related technical experience who's ready to take ownership of core QMS processes — whether you're deepening your medical device Quality expertise or transitioning in from another regulated or technical field. How We Work We are intentional. We prioritize and are thoughtful about how we use others' time. We care for others. We prioritize safety both for patients and one another. We own outcomes, not just tasks. Our work demands the highest standards because it impacts real patients and real lives. Humility is a strength. We are honest about what we know and what we don't know. Getting it right matters more than being right.

Requirements

• Bachelor's degree in a technical, scientific, or engineering discipline, or equivalent practical experience.
• 2–4 years of experience in a quality, manufacturing, or related technical role.
• Experience working in electronic QMS/PLM platforms (Arena PLM preferred).
• Strong attention to detail, clear written and verbal communication, and comfort managing multiple concurrent tasks and shifting priorities in a fast-paced startup environment.

Nice To Haves

• Experience in regulated environments, particularly medical devices (ISO 13485) and medical device software (IEC 62304).
• Experience with computer software assurance for production and quality management system software.
• Experience with supplier quality management, incoming inspection, and/or receiving inspection processes.
• Experience with dimensional inspection and/or vision inspection systems.
• Familiarity with statistical techniques (e.g., SPC, sampling plans).

Responsibilities

• Own day-to-day Arena administration and support ongoing improvement of Arena workflows in alignment with applicable regulations.
• Own computer software assurance (software validation) activities for software tools used in development and quality processes, including risk-based validation planning and execution.
• Administer change control activities and change implementation, partnering with Engineering subject matter experts to improve documentation quality, clarity, and accuracy.
• Perform receiving and inspection activities for incoming parts and materials, including dimensional inspection, documentation, and disposition — providing coverage and faster turnaround alongside the Quality Manager.
• Support supplier management activities, including qualification documentation, audit preparation and tracking, and supplier communications.

Benefits

• Competitive base salary with equity
• 100% of healthcare coverage for you and your dependents
• Generous vacation policy
• Paid parental leave
• Work from our beautiful waterfront office in Alameda, CA, with access to collaborative spaces and labs

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level