Senior QA Learning Administrator

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

The role:

Are you ready to join an elite team and make a meaningful impact? At Lonza AG, we are looking for a dedicated Senior QA Learning Administrator to help us maintain outstanding standards in our Learning Management System (LMS). This role offers an exceptional opportunity to be at the forefront of our compliance and training efforts, ensuring our team operates flawlessly!

This role is best suited for someone who ideally has Cornerstone expertise and has worked within a GMP Good Manufacturing Practice (GMP).

1. Support day-to-day Quality Assurance activities by approved Standard Operating Procedures (SOPs) and Policies for a GMP facility.
2. Maintain availability of template documents for new starters, internal transfers, and employees changing roles, and update the LMS to reflect the completion of these documents.
3. Make real-time decisions on process events on the floor based on knowledge of defined SOPs and Policies.
4. Maintain a good understanding of GMP compliance.
5. Assist in deviation investigations, change controls, and Corrective and Preventive Action (CAPA) implementation.
6. Responsible for supporting regulatory inspections and customer audits as required.
7. Work directly with department points of contact to identify efficient and actionable structure changes to training requirements that can scale to changes in headcount and reporting lines.

1. Preferably a BA or BSc or equivalent experience in Life Sciences, IT, or Education.
2. Extensive experience in using an LMS package, preferably Cornerstone.
3. Previous experience working within a GMP environment or an equivalent regulated environment.
4. Well-Organised and used to handling large volumes of paper records.
5. Experience working as an active member of the team, generously sharing information and knowledge with others in the team.