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