• Provide high-quality toxicological support for new and existing products
• Perform literature and database searches to retrieve toxicological data
• Review, analyze, and document safety data for ingredients, products, and technologies
• Prepare ingredient monographs, toxicological assessments, safety statements, and product summaries
• Summarize risk assessment data on various toxicological endpoints
• Identify, analyze, and report project-relevant data from secondary sources and databases
• Respond to consumer queries and regulatory agency questions with scientific accuracy
• Ensure all reports contain latest, accurate, and relevant toxicological information
• Work independently and collaboratively in project-specific teams
• Actively participate in team discussions and knowledge-sharing activities
• Master’s degree in Toxicology / Pharmacology / Life Sciences or related discipline
• 1–2 years of relevant experience in toxicology or safety assessment
• Experience in on-demand research or regulatory support preferred
• Strong domain knowledge in Toxicology
• Hands-on experience with toxicological and regulatory databases (ECHA, PCPC, EFSA, Toxplanet, Embase, PubMed, etc.)
• Excellent scientific report writing and documentation skills
• Strong written and verbal communication skills
• Ability to work autonomously in a fast-paced environment
• Proficiency in MS Office (PowerPoint, basic Excel)
• Strong internet research and data screening skills
• A reputed, globally leading pharmaceutical organization
• Focused on ensuring product safety through scientific excellence
• Offers a performance-driven environment with strong learning and growth opportunities
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