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.
As a Specialist, QA (CGT) at Lonza, you will support day-to-day Quality Assurance activities in accordance with approved SOPs and policies for a multi-product, cGxP contract manufacturing facility. You will play a key role in providing QA oversight for operations, compliance, and documentation, ensuring that products meet the highest quality standards and are released on time.

• Review executed batch records, logbooks, and documentation to ensure compliance with cGMP and GDocP.
• Compile lot genealogy and disposition packages to drive timely product release.
• Provide QA oversight for product status, shipping documents, and quality tag-out systems.
• Support and approve deviation investigations, CAPA implementation, and timely closure of quality events.
• Oversee and approve changes to operational documents (e.g., MBRs, SOPs, Forms, Logbooks).
• Participate in QA shopfloor activities, changeovers, walkdowns, and audits (regulatory/customer).
• Lead and coordinate site projects, investigations, and change controls as needed.