Location: Girona | Full-time | Pharmaceutical Manufacturing
We are supporting a pharmaceutical organisation in the Girona area looking to appoint a Quality Control Supervisor – Stabilities to take ownership of stability studies and analytical method validation within a GMP-regulated environment.
This is a hands‑on role focused on coordinating stability programmes, ensuring compliance, and working closely with Regulatory Affairs and cross‑functional teams to support product lifecycle and registration activities.
You will play a key role in planning, supervising and reviewing stability studies and analytical validation activities, while overseeing day‑to‑day QC laboratory operations.
Key responsibilities include: