Toxicology / Regulatory consultant (pharma)

Requirements

Proven experience in toxicology within the pharmaceutical industry (mandatory)

Hands‑on experience in preparing products for EU market authorization

Strong knowledge of EU regulatory requirements and guidelines related to toxicology

Key Responsibilities

Provide toxicological expertise to support the development and registration of new pharmaceutical products

Support risk assessment and safety evaluation of active substances and formulations

Prepare and review toxicological documentation required for market entry in the European Union

Contribute to regulatory strategy related to toxicology for EU submissions

Collaborate with regulatory, R&D, and quality teams during product launch preparation

Employment Type:

Part‑time, consultancy‑based

Location:

Fully remote

If you are interested in such opportunity please feel free to contact us to hr@asasw.ch

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