- Location
- Saclay, Île-de-France, France · published
- Department
- Operations
- Source
- Workable
Description
Join Excelya, where Audacity, Care and Energy define who we are and how we work. We believe in creating ambitious solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.
This role offers an exciting opportunity to join a dynamic and ambitious team supporting drug development programs from preclinical stages through market authorization. You will provide toxicology expertise related to impurity assessment, genotoxicity strategies, and health-based exposure limits within a highly collaborative and regulated environment.
Key Responsabilities :
- Support non-clinical safety strategies related to drug impurities, extractables & leachables, and genotoxic impurities.
- Assess and qualify impurities throughout the drug development lifecycle in accordance with ICH Q3A/B/C and ICH M7 guidelines.
- Develop impurity risk assessments and support safety evaluations.
- Contribute to the preparation of regulatory documentation and scientific justifications.
- Provide toxicological expertise for the management of potential genotoxic impurities.
- Calculate Permitted Daily Exposures (PDEs) and other health-based exposure limits.
- Support occupational toxicology activities, including the derivation of occupational exposure limits.
- Collaborate closely with CMC teams, external partners, and cross-functional project stakeholders.
- Communicate toxicology strategies and recommendations effectively across project teams.