Main tasks:

• 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.
• Summarize an...