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.

Lonza AG is offering an outstanding opportunity to become a Quality Control Compliance Specialist in New Hampshire, USA. The incumbent will play a pivotal role in ensuring detailed compliance with GMP documents and identifying as well as resolving quality issues. This position allows you to provide outstanding insight to internal customers and effectively serve as a role model for others on the team. Join our high-reaching team and give to Lonza’s validated reputation in healthcare manufacturing.

Key responsibilities:

• Apply an identified standard to independently review and approve documents such as SOPs, Master Batch Records, Work Instructions, Test Methods, Specifications, Forms, Checklists, and Scanned Documents within the Document Management System




• Assess events to resolve possible impacts on regulatory and operational compliance.




• Document review observations and suggest edits/comments when applicable.




• Follow Lonza’s documentation review procedures and ensure changes are rationalized appropriately and accurately reflected in documents.