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.

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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