Who We Are
We touch the lives of over 200 million patients every day, and billions every year. After all, everyone needs healthcare or medication at some point. Yet until today, you may not have heard of us. We're Teva, a global pharmaceutical company, committed to increasing access to high-quality healthcare to patients around the world and we currently have a fantastic opportunity for a Engineering Validation Manager to join our team on a Full Time, Permanent basis in Runcorn.
At Teva Runcorn, we develop, manufacture and market innovative and affordable medicines, specialising in sterile liquid products mainly used for treating respiratory conditions using Blow-Fill-Seal technology as well as injectable Combination Products such as our MS treatment Copaxone.
The Opportunity
The Engineering Validation Manager has responsibility for leading and directing all equipment requalification and specific initial qualification activities across the Runcorn site. This role plays a critical part in maintaining regulatory compliance and operational excellence. The position develops and directs a team of validation professionals and is accountable for strategic planning, scheduling and execution of validation activities with key cross-functional stakeholders. A strong emphasis is placed on planning, execution, and building a capable, responsive, and future-ready team.
How You'll Spend Your Day