The Clinical Release and Stability (CRS) department, part of Chemical and Pharmaceutical Development & Supply – Analytical Development, supports the R&D portfolio by conducting analytical testing.
Key Responsibilities:
- Perform analysis to support product characterization, method validation, release, and stability testing, with a strong focus on Liquid Chromatography (LC).
- Ensure compliance with all relevant regulations, analytical methods, GMP, and safety standards.
- Scientifically evaluate generated results.