Analytical Associate in Analytical Development for Synthetic Molecules

Tasks & Responsibilities:

• Development and optimization of robust analytical methods (e.g., HPLC, GC, LC-MS, GC-MS, KF) for the quality assessment of starting materials, intermediates, and active pharmaceutical ingredients (APIs).
• Planning and meticulous execution of experiments, including reaction monitoring and method development.
• Close collaboration with process development and cross-functional partners to coordinate analytical activities and sample management.
• Close cooperation with the QC (Quality Control) unit to ensure a smooth transfer of the developed analytical methods.
• Creation of high-quality documentation, including analytical procedures and reports that serve as the foundation for method validations and regulatory filings.
• Application of an innovative mindset and digital tools for continuous improvement of analytical workflows in a dynamic environment.