• Conduct in-vitro ADME studies including solubility, stability, plasma protein binding, metabolic stability, drug–drug interaction studies, and Caco-2 permeability assays
• Perform bioanalytical sample preparation and support LC-MS/MS data acquisition and integration
• Record raw data accurately and perform data acquisition, compilation, analysis, and scientific interpretation
• Ensure data integrity, accuracy, and compliance with SOPs and quality standards
• Prepare study plans, protocols, and detailed study reports
• Maintain laboratory instruments, equipment, and work areas as per approved SOPs
• Execute assigned experimental work independently with minimal supervision
• Follow laboratory safety, quality, and documentation practices consistently
• Master’s degree in Pharmacy, Biotechnology, Chemistry, Biochemistry, or a related discipline
• 1–4 years of relevant experience in in-vitro ADME and bioanalytical studies
• Hands-on experience with in-vitro ADME assays
• Practical knowledge of LC-MS/MS techniques
• Strong understanding of bioanalytical sample preparation and data analysis
• Knowledge of laboratory SOPs, GLP principles, and data integrity requirements
• Strong analytical, documentation, and reporting skills
• Ability to work independently with attention to detail
Eurofins is a global leader in laboratory testing and bioanalytical services, supporting pharmaceutical, biotechnology, and healthcare industries worldwide. With a strong focus on quality, scientific excellence, and regulatory compliance, Eurofins provides end-to-end solutions across drug discovery, development, and safety assessment.
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