Toxicological risk assessment of impurities and excipients in pharmaceutical productsEvaluation 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 evaluationDeveloping safety rationale for setting impurity specifications for pharmaceutical productsExplore publicly available literature to support developing safety rationale for unstudied chemicalsEnvironmental risk assessment of pharmaceuticalsHealth hazard assessment / health risk assessment to address product quality issues and to support product recall decisionsPermitted daily exposure (PDE) and occupational exposure limit (OEL) derivationRequired 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
Skills Required
qsar, Environmental Risk Assessment, clinical services