4.0 - 6.0 years

3 - 7 Lacs

Hyderabad, Telangana, India

On-site

Key Responsibilities 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

Posted 3 weeks ago

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Research Associate - Pre-Clinical Cadila Pharmaceuticals

2.0 - 5.0 years

3 - 5 Lacs

Dholka

Work from Office

Role & responsibilities 1. Act as Study Director for various Pre-Clinical studies as per guidelines 2. Conduct, schedule & report toxicological studies for various products in pre-clinical studies 3. Conduct a Pharmacological evaluation of various pharmaceutical products 4. Preparation of SOP & documentation as per guidelines 5. Ensuring facility readiness as per regulatory guidelines & audits

Posted 1 month ago

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