Toxicological Risk Assessment:
Evaluate impurities and excipients in pharmaceutical products to assess potential health risks.
Structure-Activity Relationship (SAR) Evaluation:
Analyze chemical structures using Structure-Activity Relationship methods, including Quantitative Structure-Activity Relationship (QSAR) models, to identify health hazards in unstudied compounds.
Read-Across Evaluation:
Identify structural analogues and develop scientific rationales to support read-across assessments for untested chemicals.
Impurity Specification Development:
Develop safety justifications for setting impurity specifications in pharmaceutical products.
Literature Exploration:
Conduct thorough reviews of publicly available scientific literature to support safety assessments for unstudied chemicals.
Environmental Risk Assessment:
Perform environmental risk assessments for pharmaceutical compounds in accordance with regulatory standards.
Health Hazard Assessment:
Conduct health hazard and risk assessments to address product quality issues and support decision-making for product recalls, when necessary.

Strong understanding of toxicological and pharmacological principles
Experience with QSAR, read-across techniques, and scientific literature evaluation

Senior Specialist,