Descripción de la oferta
Location : Girona | Full-time | Pharmaceutical Manufacturing
We are supporting a pharmaceutical organisation in the Girona area looking to appoint a Quality Control Supervisor to take ownership of batch release and QC laboratory oversight within a GMP-regulated environment.
This is a hands‑on role focused on ensuring the timely and compliant release of product, working closely with QA and manufacturing.
The Role
You will play a key role in reviewing and approving analytical data to support batch release, while overseeing day‑to‑day QC laboratory activities.
Key responsibilities include :
Reviewing and approving analytical results to support batch release
Ensuring all QC activities are completed in line with GMP and regulatory requirements
Supervising and coordinating QC laboratory operations (chemical and / or microbiology)
Managing and reviewing deviations, OOS / OOT investigations and CAPAs
Acting as a key interface between QC, QA and production to ensure timely product release
Supporting regulatory inspections and internal audits
Driving improvements in lab efficiency, compliance and turnaround times
Your Profile
We’re looking for someone with strong experience in QC within a GMP environment, with particular exposure to batch review and release processes.
You will likely have :
Experience working in a GMP-regulated QC laboratory
Direct involvement in batch release, or review of analytical data supporting release
Experience handling deviations, investigations and CAPAs
Exposure to supervising, coordinating or mentoring team members
Strong understanding of analytical testing (e.g. HPLC, microbiology, stability)
Familiarity with systems such as LIMS, Trackwise or similar
Why Apply
High‑impact role with clear ownership of batch release activities
Opportunity to step into or develop leadership responsibilities
Collaborative GMP environment with strong cross‑functional exposure
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