At Flow Neuroscience, we’re building the future of mental health treatment — combining neuroscience, hardware, and software to deliver clinically proven, non-drug therapy at scale.
Our flagship product, the Flow FL-100, is an at-home treatment for major depressive disorder, one of the leading causes of disability worldwide. It is the first neuromodulation treatment FDA-approved as a standalone, at-home treatment for major depressive disorder.
Following regulatory approvals in Europe, UK, Australia, and the US, we’re entering a new phase of growth — scaling manufacturing, strengthening our quality systems, and expanding globally.
We’re now looking for a Senior Medical Device Quality Assurance & Regulatory Engineer to take a central role in maintaining and evolving our QA, QMS, and regulatory infrastructure.
The RoleYou will own and drive critical parts of our quality and regulatory framework across the full product lifecycle — from design and development through manufacturing at our contract manufacturers, post-market, and supporting regulatory submissions. You will act as the technical owner for key product lifecycle and quality processes, driving cross-functional projects across R&D, manufacturing, quality and regulatory.
This is a high-impact role at the intersection of engineering, manufacturing, quality, and regulatory strategy. You will be embedded within our technical teams and work closely with Quality, Regulatory, and Supply Chain.
What You’ll DoLead and maintain Design Control processes (design history file, verification/validation, risk management, device change control)
Own and maintain Technical Documentation / Technical Files / DHFs / DMRs
Drive supplier qualification, auditing, and ongoing manufacturing quality control and improvements
Collaborate closely with R&D on design changes and process improvements
Support and continuously improve our ISO 13485-certified QMS
Support regulatory submissions and updates (EU MDR, FDA)
Ensure compliance with evolving regulations, including FDA QMSR, EU and UK MDR changes
Support audits (Notified Body, FDA, suppliers, internal) and inspection readiness
Work cross-functionally with product, regulatory, and operations teams
You’re someone who understands both the letter of the regulations and the reality of building a product in a fast-moving company. You have a strong technical background in either medical-device software or hardware/product engineering, combined with hands-on experience in medical-device design, development and manufacturing.
Core CompetenciesVery strong technical project management skills
Strong technical experience with active medical devices
Strong understanding of design and development controls under ISO 13485 and FDA QMSR (21 CFR Part 820)
Hands-on experience with supplier and manufacturing quality control
Proven experience managing Technical Files / DHF / DMR
Expertise in ISO 13485 QMS implementation and maintenance
Experience with FDA regulations (QMSR) and EU MDR
Experience with FDA inspections and/or Notified Body audits
Experience with FDA PMA devices (Class III) and PMA supplements
Background in combination hardware/software medical devices
Quality management system automation, eQMS & AI-tools.
Experience working closely with Asia-based contract manufacturers
Experience working with neurotech.
You take ownership and operate with high autonomy
You’re structured, detail-oriented, and pragmatic
You can translate regulatory requirements into efficient processes
You enjoy working cross-functionally with engineers and operators
You’re comfortable in a scaling environment where not everything is fully defined, and you enjoy building the processes and systems that are missing
Work on a clinically proven treatment for one of the world’s largest health problems
Be part of a company transitioning into global scale (including the US market)
Own meaningful parts of the quality and regulatory backbone of a US Class III device
Join a mission-driven team combining science, engineering, and real-world impact
Location: Hybrid. Skåne, Sweden, or London, UK. You will be expected to work from one of our offices a few times per week.
