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Stéphanie H.SH

Stéphanie H.

Expert Quality Systems / Regulatory Compliance

On-demand
Strasbourg, FR
15+ years

Average response time: 1 hour

Freelancer profile translated to English.
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About Stéphanie

Industrial Pharmacistwith over 15 years of experience in the Pharmaceutical and medical device industry,expert in quality systemsand their implementation to meet current regulations, convinced that aQuality Cultureis fundamental to enhancing the work of teams and integrating the patient's perspective into decisions.

**Passionate about the diversity of product typologies offered by the pharmaceutical or medical device industry**, after having sought to understand yours in depth, I will be able to adapt regulatory requirements to make their execution relevant for you.

  • English

    Fluent

  • German

    Conversational

  • French

    Native or bilingual

Can work on-site
Strasbourg (up to 50km), Paris (up to 10km)

Experience

  • RDS (Rhythm Diagnostic Systems)
    Quality Assurance Regulatory Affairs Director, PRRC and DPO
    MEDICAL
    June 2020 - February 2025 (4 years and 8 months)
    Strasbourg, France
    Member of the Company Leadership team as QARA Director Successful QMS implementation from scratch (from definition to implementation followed by training) Definition of a regulatory strategy to put an active medical device on the EU market (CE marking) and on the US market (510(k) clearance) Lead successful CE marking project from notified body selection and management to compliant technical documentation and QMS issuance Data Privacy Officer for health data processed by the medical device Budget management, skills=[]
  • Catalent Pharma Solutions
    Data Integrity (DI) and Data Governance (DG) specialist
    PHARMACEUTICALS INDUSTRY
    October 2018 - June 2020 (1 year and 8 months)
    Strasbourg, France
    Implementation of a DI culture (robust processes, clear procedures, DI tools, trainings) Support for the implementation of the new DI processes on site Supervision of the DI remediation action plan and of DG processes, skills=[]
  • Catalent Pharma Solutions
    Supplier QA
    PHARMACEUTICALS INDUSTRY
    February 2018 - October 2018 (8 months)
    Strasbourg, France
    Risk based supplier management process definition Supplier audit Quality agreements negotiations New material introduction, skills=[]

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Education

  • Doctor of Pharmacy
    Faculty of Pharmacy of Strasbourg
    2010
  • Master 2 Pharmaceutical Protein Engineering
    Graduate School of Biotechnology of Strasbourg
    2010

Certifications

  • IRCA Lead Auditor
    BSI
    2025
    Audit ISO 13485 ISO Certification Internal Audit

Skill set

Categories

  • Other