Madrid, Spain Call4Entrepreneurs
- The Collider About the job CTO BraidStent (The Collider Programme) CTO — BraidStent Lead the technical build of a first-in-class medical device, from spin-off to CE Mark. BraidStent is a biodegradable ureteral stent developed at IRYCIS (Instituto Ramón y Cajal, Madrid), one of Spain's leading biomedical research institutes, under the scientific leadership of Dr. Federico Soria. Backed by over a decade of research and a strong publication record, the technology addresses a well-documented unmet need in one of the most common urological procedures worldwide.
Currently, the project is part of The Collider's Venture Building programme, with spin-off incorporation planned for late ****. We're looking for a hands?on CTO to join the founding team and take the technology from validated science to a scalable, regulatory-compliant product. Current founding team:
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Location:
Europe, ideally Madrid or Barcelona. Hybrid/remote, with regular travel to manufacturing and testing partners.

What you'll do
Define and run the manufacturing process for components, assembly, sterilisation and packaging, with contract manufacturers and suppliers, under ISO * and MDR. Own quality: raw material specs, incoming QC, supplier qualification, release criteria, traceability and batch records. Testing & regulatory Lead pre-clinical validation (bench, in-vitro, in-vivo) with the CSO, and maintain the device specification linking design inputs, risk controls and V&V.; Build and maintain the ISO * QMS and the MDR technical file (design history,



ISO * risk management, V&V; evidence); support Notified Body interactions and the CE Mark submission. Contribute to early US regulatory strategy (510(k)/De Novo) for future expansion. Team & partners Select and manage CMOs, test labs and other technical providers. Translate research outputs and clinical feedback into regulatory-grade documentation and design improvements, working closely with the CSO and CEO. What we're looking for Degree in biomedical engineering, materials science, polymer or mechanical engineering, or related field. 3+ years hands?on in Class IIb/III medical device development and manufacturing. Implantable or minimally invasive devices a plus. Proven experience implementing an ISO * QMS and preparing MDR technical documentation (Annex II/III) through Notified Body review. Working knowledge of ISO * risk management and design-control principles. FDA experience (510(k), De Novo or PMA) is a strong plus. Comfortable in a startup environment; fluent in Spanish and English.

What we offer
Founding team membership with equity, milestone-based vesting. The chance to lead technical development of a first-in-class device from spin-off to CE Mark. Base salary from company incorporation, in line with experience. Versátil

working hours
; open to part-time or phased incorporation, especially during the pre
- and early post-constitution period. A collaborative deep-tech ecosystem, with clinicians, researchers, and incubator/accelerator partners. #J-*-Ljbffr

📌 Head of Technology (España)
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📍 España