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Toxicology / Regulatory consultant (pharma)
Zusammenfassung
A pharmaceutical consultancy is seeking a part-time toxicologist for remote work to provide expertise in the development and registration of new products. Responsibilities include preparing toxicological documentation, supporting safety evaluations, and contributing to regulatory strategies for EU market authorization. Candidates must have proven experience in toxicology within the pharmaceutical sector and a strong understanding of EU regulations.
Qualifikationen
- Proven experience in toxicology within the pharmaceutical industry.
- Strong knowledge of EU regulatory requirements and guidelines.
- Hands-on experience in preparing products for EU market authorization.
Aufgaben
- Provide toxicological expertise to support the development of new pharmaceutical products.
- Support risk assessment and safety evaluation of active substances.
- Prepare and review toxicological documentation for EU market entry.
- Contribute to regulatory strategy for EU submissions.
- Collaborate with teams during product launch preparation.
Kenntnisse
- 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
- 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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