Berlin, Germany · On-site
$100k–$130k/yr
Your mission About DeepSpin Today, 7 out of 10 people globally lack access to life-saving Magnetic Resonance Imaging (MRI). Conventional MRI machines are massive, cost millions of euros, and require specialized, shielded…
Skills: Regulatory Affairs, Quality Assurance, FDA 510(k) Submission, CE Certification, ISO 13485
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Lead medical device certification for MRI systems in the US and Europe, specifically driving FDA 510(k) and CE Class IIa processes. Manage and continuously improve the Quality Management System (QMS) in compliance with ISO 13485 and FDA regulations.
Requires a degree in Life Sciences or Engineering with over 7 years of regulatory experience in the medical device industry. Must have a proven track record of taking Class II devices through FDA or CE certification processes.
Today, 7 out of 10 people globally lack access to life-saving Magnetic Resonance Imaging (MRI). Conventional MRI machines are massive, cost millions of euros, and require specialized, shielded rooms which means they are usually confined to large hospitals.
At DeepSpin, we are changing that by building the World’s First Flatbed MRI.
Our open-architecture scanner plugs into a standard wall socket, fits into regular doctor's offices, and costs 10x less than conventional systems.
Backed by globally leading VCs, we are expanding our team in Berlin. This is an opportunity to join a mission-driven team bringing an essential medical technology to the billions of people who currently cannot afford it.
As our Regulatory Affairs & Quality Assurance Manager, you will lead the medical device certification for our MRI system in the US and Europe, while managing and improving our Quality Management System (QMS).
This is a key role where you will have direct ownership of our regulatory strategy and play a major part in bringing our product to market.
Certification: Drive the CE Class IIa medical device certification and FDA 510(k) submission processes.
Documentation: Author, review, and maintain technical documentation for regulatory submissions; including Design History Files (DHF), Device Master Records (DMR), Risk Management Files, and usability data (IEC 62366).
Compliance & Risk: Lead risk management activities according to ISO 14971, and manage product testing for electromagnetic safety/compatibility, cybersecurity, and biocompatibility.
QMS Management: Define, implement, and continuously improve our QMS processes in line with ISO 13485 and FDA regulations.
Gap Analysis & Technical Collaboration: Conduct gap analyses to identify areas needing improvement and implement corrective actions. Partner with engineering staff on design review meetings, SOPs, work instructions, and V&V testing.
External Liaison: Act as the primary contact and coordinate with notified bodies (TÜV, FDA, LaGeSo) and competent authorities.
Post-Market & Infrastructure: Support post-market surveillance, vigilance, and complaint handling (ensuring timely reporting under 21 CFR 803). Help build a simplified, practical reporting infrastructure that satisfies regulatory needs.
About You
You are an independent, self-organized regulatory professional who enjoys working across teams and wants the challenge of bringing a complex physical and digital product to market.
Education: A degree in Life Sciences, Engineering, or a related technical field.
Experience: 7+ years of hands-on regulatory experience in the medical device industry.
Track Record: Proven success taking a Class II medical device through the FDA 510(k) or CE certification process.
Standards & Testing: Deep knowledge of ISO 13485 and experience managing product testing for electromagnetic safety, cybersecurity, and biocompatibility.
Relationship Management: Experience engaging and working directly with notified bodies and authorities.
Communication: Clear written and verbal communication skills in English.
Accreditation as an auditor.
Training or experience as a Risk Manager (ISO 14971).
Experience with clinical evaluations.
A technical interest in how MRI technology works.
Compensation: A total package value of up to €130,000/year (consisting of an €80,000 - €90,000 base salary + benefits+ stock options).
Culture: A creative, collaborative workplace with flat hierarchies and open communication.
International Team: An English-first office with over 10 different nationalities driven by the same purpose.
Perks: Work from our penthouse office, enjoy company-sponsored lunches, regular team events, and access to Urban Sports Club, BVG (public transport), and lifestyle vouchers.
Development: High responsibility from day one, internal mentorship, and support for external training or certifications.
Balance: 30 days of paid annual leave and flexible working hours.
Relocation: Support with visas, relocation logistics, and help finding local daycare for your children.
Next-generation MRI systems
DeepSpin is developing a next-gen, AI-powered MRI imaging machine at a fraction of the cost, size and weight of standard systems. Unleashing the power of generative topological design for our hardware and super-resolution deep learning on MRI images, we are taking medical imaging to the digital age. Through our proprietary technology, we will be making MRI accessible to every patient globally. Join us in the journey to becoming the imaging standard of care in a myriad of previously inaccessible medical domains.
Offices: Berlin, DE
View all jobs at DeepSpinNext-generation MRI systems
DeepSpin is developing a next-gen, AI-powered MRI imaging machine at a fraction of the cost, size and weight of standard systems. Unleashing the power of generative topological design for our hardware and super-resolution deep learning on MRI images, we are taking medical imaging to the digital age. Through our proprietary technology, we will be making MRI accessible to every patient globally. Join us in the journey to becoming the imaging standard of care in a myriad of previously inaccessible medical domains.
Offices: Berlin, DE
View all jobs at DeepSpin