- Experience required in Quality Control Laboratory and investigation of OOS/OOT/LIR/OOC, with expertise in reviewing analytical documents such as AMV protocols and reports.
- Experience with analytical techniques like HPLC, GC, FTIR, and UV-Vis spectroscopy.
- Prior exposure to quality management systems and laboratory automation tools.
- Perform detailed investigations for OOS, OOT, LIR, and OOC results.
- Identify root causes and propose effective corrective and preventive actions (CAPA).
- Document investigation outcomes clearly and ensure timely resolution.