European SDS & Regulatory Compliance Specialist

DKSH

Lyon

Sur place

EUR 65 000 - 90 000

Temps partiel

14 jours+
Générateur de candidature

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Résumé du poste

DKSH in Europe seeks a Specialist, Chemical Product Safety Europe to ensure compliance, labeling and safety documentation for chemical products across the EU, UK, and Switzerland. You will contribute within a 12-person regulatory team to protect product integrity and support DKSH's European network.

The role is based in multiple European hubs including Miribel, Barcelona, Porto or Warsaw, with a focus on CLP classifications, SDS authoring and ongoing regulatory monitoring.

Qualifications

  • Master's degree in Chemistry, Biology, Toxicology, Ecotoxicology, or a related discipline.
  • 3 to 5 years of experience in Health, Safety, and Environment (HSE), SDS authoring, and chemical product regulations (including REACH and CLP).
  • Proficient in English; proficiency in another European language is a plus.

Responsabilités

  • Analyze data to support risk prevention and hazard assessment.
  • Determine classification of substances and mixtures per CLP, UK and Swiss rules.
  • Assess dangerous goods classification per ADR, IMDG, IATA.
  • Author and maintain SDSs and CLP labels for DKSH Europe.
  • Review suppliers SDSs, product compositions and data for compliance gaps.
  • Monitor evolving chemical regulations to ensure ongoing compliance.
  • Notify classified mixtures to Poison Control Centers across Europe.
  • Educate internal stakeholders on hazard management and labeling.

Connaissances

English proficiency
Team collaboration
Regulatory mindset
Stakeholder communication

Formation

Master's degree in Chemistry or related discipline

Description du poste

DKSH in Europe seeks a Specialist, Chemical Product Safety Europe to ensure compliance, labeling and safety documentation for chemical products across the EU, UK, and Switzerland. You will contribute within a 12-person regulatory team to protect product integrity and support DKSH's European network.

The role is based in multiple European hubs including Miribel, Barcelona, Porto or Warsaw, with a focus on CLP classifications, SDS authoring and ongoing regulatory monitoring.

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