Quality Control Supervisor – Stabilities

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, technical reports and regulatory documentation linked to stability and validation
• Monitoring study timelines, identifying risks and ensuring on-time delivery of results
• Acting as a key interface between QC and Regulatory Affairs to support registration and submission activities
• Performing data checks and ensuring accuracy of stability testing results
• Managing deviations, investigations and CAPAs within the QC environment
• Ensuring all activities are carried out in compliance with GMP and quality standards
• Supporting audits and regulatory inspections
• Driving continuous improvement in laboratory processes, efficiency and compliance

Your Profile

We’re looking for someone with strong experience in QC within a GMP environment, with particular exposure to stability studies and analytical method validation.

You will likely have:

• Experience working in a GMP-regulated QC laboratory
• Hands-on involvement in stability studies (ICH) and/or analytical method validation
• Experience reviewing technical documentation, protocols and reports
• Exposure to deviations, investigations and CAPAs
• Experience supervising, coordinating or mentoring laboratory teams
• Strong understanding of analytical techniques (e.g. HPLC, ELISA, microbiology or similar)
• Familiarity with systems such as LIMS, Trackwise or similar

Why Apply

• High-impact role with ownership of stability programmes and validation activities
• Opportunity to step into or develop leadership responsibilities
• Strong exposure to Regulatory Affairs and product lifecycle activities
• Collaborative GMP environment with cross-functional visibility