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Pierre CharlierPC

Pierre Charlier

Medical product design & validation

€600/day
Lille, FR
8-15 years

Average response time: 1 hour

Freelancer profile translated to English.
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About Pierre

An engineer for 10 years and founder of Orbivia, I support companies in the development of their electronic products. My approach is pragmatic: design, test, and manufacture, without superfluous intermediaries.

🛠️ Why work with me?
I have my own workshop in Lille, which allows me to be very responsive in iterating on your prototypes:
  • 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.)


🎯 Examples of achievements:
Health: High-criticality brain monitoring system (EEG/NIRS/PPG) for the operating room.
Tech: Miniature voice Bluetooth assistant with AI, UV sensors, drone detector.
Industry: Pyrotechnic testers, robust photo booths, NFC readers.
Have a prototype or finished product project? Let's discuss it.
  • French

    Native or bilingual

  • English

    Fluent

Can work on-site
Lille (up to 50km)

Experience

  • ORBIVIA
    CEO ORBIVIA
    May 2025 - Today (1 year and 3 months)
    Lille, France
    Support for companies and project leaders in the development, pre-production, and compliance of R&D projects.
    Electronic Design CE Marking Research and Development R&D IEC 60601 ISO 13485
  • Braindex
    Technical Director
    BIOTECH
    January 2020 - May 2025 (5 years and 4 months)
    Loos, France
    Led 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.
    Project Management EEG NIRS Industrial Design medical device
  • Cic it (Secteur Médical)
    Research Assignment Manager
    MEDICAL
    January 2016 - December 2019 (3 years and 11 months)
    Lille, France
    Research 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.
    ECG Signal Processing Clinical Research Research and Development R&D ISO 9001

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Education

  • PhD in Biotechnology
    University of Lille
    2019

Certifications

  • Medical Device Expertise - ISO 13485
    Isocèle conseil
    2025
  • Medical Software - IEC 62304
    MD101
    2021

Skill set

Categories