Qualification & Calibration Manager (Madrid)

Your Role

As the owner of a site-wide Qualification and Calibration (Q&C;) program in a GMP-regulated biopharmaceutical manufacturing environment, you will shape the strategic direction and operational performance of a function central to product quality and regulatory compliance. You will lead a team of specialists and supervisors, own both the Qualification Master Plan and the Calibration Master Plan, and serve as the primary subject matter expert during regulatory inspections. As an active member of the Engineering and Maintenance leadership team, you will drive continuous improvement through data‑driven approaches and digital tools, manage external service providers, and champion a culture of accountability and operational excellence across the manufacturing site.

Who You Are

• You bring a minimum of 8 years of experience in a GMP-regulated pharmaceutical, biopharmaceutical, or medical device manufacturing environment, including at least 5 years of...