About Pierre
- Electronics: Design of boards and in-house assembly on my own automatic SMT line.
- Mechanics: 3D printing of your enclosures with technical materials or laser cutting.
- Testing & Validation: I am equipped in-house with the necessary laboratory equipment to pre-test, debug, and validate developed systems.
- Compliance: Accustomed to demanding regulatory constraints, particularly in the medical sector (ISO 13485, 60601-1, 14971, 62304 standards, etc.)
French
Native or bilingual
English
Fluent
Experience
- ORBIVIACEO ORBIVIAMay 2025 - Today (1 year and 3 months)Lille, FranceSupport for companies and project leaders in the development, pre-production, and compliance of R&D projects.
- BraindexTechnical DirectorBIOTECHJanuary 2020 - May 2025 (5 years and 4 months)Loos, FranceLed a multidisciplinary team for the development of a highly critical medical device (EEG / NIRS) for the operating room.
- From idea to industry: Full lifecycle management, from POC (Proof of Concept) to the implementation of the industrialization line.
- Regulatory affairs: Implementation of CE documentation in accordance with the MDR regulation and management of associated normative tests.
- Innovation: Development of a multimodal tool facilitating real-time monitoring of vulnerable patients.
- Cic it (Secteur Médical)Research Assignment ManagerMEDICALJanuary 2016 - December 2019 (3 years and 11 months)Lille, FranceResearch and development of innovative medical technologies within multidisciplinary teams.
- Fetal monitoring: Development of a non-invasive, multi-source system for continuous acquisition of fetal heart rate.
- Signal processing: Design of acquisition solutions for PPG sensors and physiological measurement systems.
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Education
- PhD in BiotechnologyUniversity of Lille2019
Certifications
- Medical Device Expertise - ISO 13485Isocèle conseil2025
- Medical Software - IEC 62304MD1012021