Today, Lonza is a global leader in life sciences operating across three 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 QC Analyst, you will be responsible for managing QC samples (receipt, retention, and shipment), coordinating on-site and off-site archival of QC documents, overseeing equipment maintenance activities, and supporting the revision of operational procedures. You will also liaise with other departments to ensure timely delivery of results, compliance with standards, and smooth execution of laboratory operations.

• Manage QC samples, including receipt, storage, retention, and discard of process and raw material samples.
• Control and audit retain samples to ensure compliance with procedures.
• Coordinate Sample Logistics documentation and QC assay sheet issuance.
• Write, maintain, edit, and review Standard Operating Procedures (SOPs).
• Maintain data and records in compliance with cGMP and internal quality standards.
• Manage and coordinate on-site and off-site archival of QC documents.
• Perform stability pull samples according to defined time points.
• Contribute to operational efficiency and continuous improvement initiatives.
• Perform other duties as assigned by Supervisor/Manager.