Senior QA Learning Administrator

Sorry, this job was removed at 06:52 p.m. (CST) on Tuesday, May 06, 2025
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Slough, Berkshire, England
In-Office
Pharmaceutical
At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization.
The Role

 

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).

Key responsibilities:

  • Support day-to-day Quality Assurance activities by approved Standard Operating Procedures (SOPs) and Policies for a GMP facility.

  • 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.

  • Make real-time decisions on process events on the floor based on knowledge of defined SOPs and Policies.

  • Maintain a good understanding of GMP compliance.

  • Assist in deviation investigations, change controls, and Corrective and Preventive Action (CAPA) implementation.

  • Responsible for supporting regulatory inspections and customer audits as required.

  • 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.

Key requirements:

  • Preferably a BA or BSc or equivalent experience in Life Sciences, IT, or Education.

  • Extensive experience in using an LMS package, preferably Cornerstone.

  • Previous experience working within a GMP environment or an equivalent regulated environment.

  • Well-Organised and used to handling large volumes of paper records.

  • Experience working as an active member of the team, generously sharing information and knowledge with others in the team.

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

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The Company
HQ: Basel
0 Employees
Year Founded: 1897

What We Do

At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization. Our community of 16,000 talented employees work across a global network of more than 30 sites to deliver for our customers across the pharma, biotech and nutrition markets.

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