The Analytical Scientist in Quality Control (QC) supports the analytical characterization of lead molecules and investigational medicinal products in clinical development. The candidate must possess a strong scientific background in Analytical Chemistry or equivalent and ideally have drug development experience, preferably within a CMC or QC setting. The candidate must have a clear record of scientific accomplishments and ability to interact across functions within a dynamic matrix organization.

Key Responsibilities

• Perform and/or coordinate the QC analytical method transfer, qualification and/or validation activities to/at external partner(s) or Contract Research Organizations (CROs), including review of required GMP documentation, for Drug Products, APIs and Starting materials
• Provide QC support (hands-on) to the Analytical Development (AD) team in the development & implementation of analytical methods intended to be transferred and executed in...