Toxicology / Regulatory consultant (pharma)

ASA Swiss; Remote; EUR 80.000 - 100.000; Teilzeit

Zusammenfassung

A pharmaceutical consulting firm is seeking a part-time toxicology expert to support market authorization of new products. The role requires proven experience in toxicology and familiarity with EU regulatory requirements. Responsibilities include providing expertise for product registration, preparing toxicological documentation, and collaborating with various teams to ensure compliance during product launches. This opportunity is fully remote, allowing for flexible work arrangements.

Qualifikationen

• Proven experience in toxicology within the pharmaceutical industry is mandatory.
• Hands-on experience in preparing products for EU market authorization is required.
• Strong knowledge of EU regulatory requirements and guidelines related to toxicology.

Aufgaben

• 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.

Kenntnisse

Experience in toxicology

Knowledge of EU regulatory requirements

Jobbeschreibung

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 [e-mail]