Manager, Clinical Services

• Toxicological risk assessment of impurities and excipients in pharmaceutical products
• Evaluation of structure-activity relationship of chemicals, including QSAR to identify the health hazards of unstudied compounds.
• Identification of structural analogues and developing rationale to support read-across evaluation
• Developing safety rationale for setting impurity specifications for pharmaceutical products
• Explore publicly available literature to support developing safety rationale for unstudied chemicals
• Environmental risk assessment of pharmaceuticals
• Health hazard assessment/health risk assessment to address product quality issues and to support product recall decisions
• Permitted daily exposure (PDE) and occupational exposure limit (OEL) derivation

Required Qualification

• Masters in pharmacology/Pharmacy or PhD in Pharmacology/toxicology
• Good understanding on principles of toxicology and pharmacology is a must

Desired Skill Set

• Experience in Toxicology studies
• Experience in risk assessment
• Experience in PDE and OEL
• Experience in Impurity qualification risk assessment
• Experience in Structure-activity relationship and QSAR
• Good written (English) communication
• Analytical thinking
• Logical and science based approach
• Attention to details