Major duties and responsibilities:
• Perform QSAR evaluations for APIs drug related impurities
• Perform risk assessment of chemical toxicophores, impurities present in drugs under development and those
in the market
• Write toxicological assessment reports and responses to regulatory agencies (i.e. response to FDA deficiency letters)

• Academic degree (MSc or PhD) in organic chemistry
• Excellent verbal and written communication skills in English
• Advanced computer skills, experience with professional cheminformatics databases
• Ability to work under stressed timelines
• Molecular modelling capabilities (QSAR)– an advantage
• Knowledge in toxicology and ADME – an advantage