Cloé Cibil Le Meudec

Angestellt, QM-QC manager Europe / Senior Global Quality Manager, Sudarshan Germany Horizons GmbH
Frankfurt am Main, Germany

Fähigkeiten und Kenntnisse

Project leader capabilities & experience. Expertis
Quality Management
English Language
Quality management DIN EN ISO 9001:2015
Auditor
Document Management System
Quality Assurance
Spanish
French
Catalan
German
ISO
FMEA
QMS
8D
Audit
Team work
Responsible
International experience
Communication skills
Enthusiasm
Flexibility
Intercultural competence

Werdegang

Berufserfahrung von Cloé Cibil Le Meudec

  • Current 10 months, since Sep 2025

    QM-QC manager Europe / Senior Global Quality Manager

    Sudarshan Germany Horizons GmbH

    QM/QC Lead Europe- Quality Manager - System Management - internal auditor - ISO Certification -

  • 3 years and 9 months, Jan 2022 - Sep 2025

    Senior Global Quality Manager

    Heubach Colorants GmbH / Sudarshan Germany Horizons GmbH

    Quality Manager - System Management - Internal auditor - ISO Certification -

  • 1 year and 5 months, Aug 2020 - Dec 2021

    Quality Manager

    Colorants Solutions Deutschland GmbH

  • 4 years and 1 month, Jul 2016 - Jul 2020

    Senior Technical Marketing Manager - Pigments

    Clariant
  • 3 years and 5 months, Feb 2013 - Jun 2016

    Application Development Manager - Personal Care

    Clariant
  • 2 years and 3 months, Nov 2010 - Jan 2013

    Development Chemist

    Colep

  • 2 years and 7 months, Apr 2008 - Oct 2010

    Formulation Scientist

    Innocoll Technologies

    Development of innovative implant & topical formulations with biopolymers. Formulation Development & Upscaling of liquid & solid formulations. Project leader: Responsible for project documentation & project planning. Documentation for medicinal products & medical devices registration in US & EU.

  • 7 months, Sep 2007 - Mar 2008

    Pharmaceutical Specialist

    Intervet - Schering Plough

    Formulation: Development of innovative solid & liquid formulations, upscaling in pilot plant, follow up of stability/pre-clinical studies. Regulatory: Answering questions to Authorities, Updating registration files for EU & US markets.

  • 6 months, Mar 2007 - Aug 2007

    Pharmaceutical Specialist assistant

    Intervet - Schering Plough

    Formulation/Analytical: Development of transdermal formulations for cattles In-vitro testing to screen formulations and analytical method validation. Follow-up of preclinical study. Regulatory: Answering questions to Authorities, Updating registration files for EU & US markets.

  • 5 months, Mar 2006 - Jul 2006

    Formulation scientist assistant

    Université de la Méditerranée, Faculté de Pharmacie

    Litterature and Patent review on gastroretentive dosage forms. Development of innovative gastroretentive dosage forms. In-vitro testing for formulation screening Follow up of pre-clinical studies (pharmacokinetic) Analytical testing of pre-clinical samples.

  • 3 months, Jun 2005 - Aug 2005

    Analytical Chemist trainee

    Sabater-Tobella Analisis

    Development & validation of HPLC method. Routine testing of stability batches for Pharmaceutical Industry.

Ausbildung von Cloé Cibil Le Meudec

  • 1 year, Sep 2006 - Aug 2007

    Université Claude Bernard Lyon 1

    Formulation Galénique / Pharmaceutique, Formulation alimentaire, Formulation cosmétique et Formulation de polymères.

  • 3 years, Sep 2003 - Aug 2006

    Institut Universitaire Professionalisé

    Université des Sciences et Technologies Montpellier 2

    Synthèse, formulation et analyse de molécules bioactives

  • 1 year, Sep 2002 - Aug 2003

    Biologie

    Université des Sciences et Technologies Montpellier 2

    Biologie / Biochimie

  • 10 months, Sep 2001 - Jun 2002

    Université de Pharmacie, Montpellier 1

Sprachen

  • French

    C2 (Verhandlungssicher / Muttersprachlich)

  • Spanish

    C2 (Verhandlungssicher / Muttersprachlich)

  • English

    C1 (Fließend)

  • German

    C1 (Fließend)

  • Catalan

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