Toxicological Risk Assessment & Report Writing

Roles & Responsibilities

• Search and retrieve toxicological data from scientific literature and regulatory databases to support safety assessment of new and existing products
• Review and document safety data for ingredients, products, and technologies used in consumer healthcare products
• Prepare toxicology sections of Ingredient Monographs, safety statements, and product summaries
• Summarize and interpret risk assessment data for key toxicological endpoints
• Identify, analyze, and report project-relevant data from secondary sources and available databases
• Respond to safety-related queries from consumers and regulatory authorities
• Ensure accuracy, relevance, and up-to-date toxicological information in all deliverables
• Work independently as well as collaboratively within project-specific teams

Qualification

• Master’s degree in Toxicology, Life Sciences, Pharmacy, or a related scientific discipline

Experience

• 1–2 years of experience in toxicological research, safety assessment, or scientific documentation

Skills

• Strong domain knowledge in Toxicology
• Experience with regulatory and scientific databases (ECHA, PCPC, EFSA, ToxPlanet, Embase, PubMed, etc.)
• Excellent scientific writing and report preparation skills
• Strong analytical and data interpretation abilities
• Proficiency in MS Office (PowerPoint, basic Excel) and internet research tools
• Good written and verbal communication skills
• Ability to work independently in a fast-paced environment

About the Organisation
The organization is a globally reputed pharmaceutical company committed to ensuring the safety of its products through robust toxicological evaluation and scientific excellence. It offers a dynamic, performance-driven environment with opportunities for learning, professional growth, and exposure to global product safety operations.