Job Description
Summary
You will be collaborating cross-functionally to drive program success and regulatory alignment, in a dynamic environment with bold corporate objectives. This is a critical role within our PharmTox team, requiring a strong scientific background and excellent communication skills to collaborate across various capabilities.
Role Responsibilities
- Provide expert scientific advice on risk assessment of potential impurities of products
- Be the single point of contact for impurity and E&L risk assessments in drug substances and drug products across the portfolio
- Be a single point of contact and support EHS by managing toxicological risk assessments linked to safety datasheets
- Outsource, guide and approve toxicological evaluations of E&L profiles associated with container closure systems, devices, and manufacturing components
- Oversee the appropriate application of risk assessment methodologies (e.g. PDE, TTC,...
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Submit ApplicationJob Details
- Location genf, genf
- Job Type Full-time
- Category Bio & Pharma & Health
- Posted Date June 28, 2026
- Application Deadline August 07, 2026