Quality Control Supervisor (Cataluña)

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.

The Role

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:

• Establishing and managing stability study plans and analytical method validation activities
• Supervising and coordinating QC laboratory operations related to stability programmes
• Reviewing protocols...

Ready to Apply?

Submit your application today and join our talented team at QP Group.