Manager (Toxicology), Development Consulting & Scientific Affairs

1 month ago


Noida, India PharmaLex Full time

Your Job

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


Your Profile

Masters in pharmacology/pharmacy or PhD in pharmacology/toxicology Good understanding on principles of toxicology and pharmacology is a must Industry experience of 5-10 years Hands on experience in: Toxicology studies Experience in risk assessment PDE and OEL Impurity qualification risk assessment Structure-activity relationship and QSAR
Desired skillset Good written (English) communication Analytical thinking Logical and science based approach Attention to details

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