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.
Your Profile
Education
Master's degree in Pharmacology or Pharmacy , or
PhD in Pharmacology / Toxicology
Expertise
Strong understanding of toxicological and pharmacological principles
Experience with QSAR , read-across techniques , and scientific literature evaluation
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