Support the analytical activities required for producing information and documentation suitable for clinical development up to Process Validation stage products with particular focus on method suitability assessment/validation/verification/transfer in accordance with GMP, ICH guidelines and the company's quality system.
Build up a strong scientific knowledge on physical and chemical technologies with particular focus on pharmacopeia requirements and global alignment.
Promote the technical innovation, scientific understanding and best practices
Design and perform experiments, interpretate results and review data for physical and chemical techniques to support method implementation/validation/verification/transfer.
Prepare validation/transfer protocols/ reports and procedures related to physical and chemical test methods. Collect and evaluate scientific data to take conclusions based on them.