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 offers an outstanding chance for a motivated candidate to become a Specialist 3, QA Raw Materials- LSA in New Hampshire, USA! This role is crucial in ensuring flawless release of essential raw materials for production.

Key responsibilities:

• Interact directly with Lonza’s suppliers and internal customers to acquire documentation required for material assessments and release.
• Independently review and approve cGMP documentation (COA, internal and external test records, BSE/TSE statements, etc.) required for material assessments and release.
• Coordinate the part number process, and lead all aspects of SAP master data review and approval.
• Manage supplier qualifications for the site effectively.
• Generate, revise, and approve material specifications.
• Facilitate the processing of vendor change notifications.
• Perform all SAP transactions required for material release as well as other quality functions within SAP.
• Manage deviations and change controls as the owner or QA approver in the Trackwise system.
• Conduct master document reviews to ensure accuracy and compliance.

Key requirements:

• Proven experience in quality assurance within the life sciences or a related industry.
• Deep understanding of cGMP documentation and regulations.
• Competence in SAP transactions and quality-related functions.
• Strong ability to manage supplier qualifications and vendor change notifications.
• Excellent communication skills to interact with suppliers and internal customers.
• Ability to perform meticulous document reviews and manage change controls.
• Bachelor’s degree or equivalent experience in a relevant field is preferred.
• Outstanding attention to detail and a dedication to maintaining high-quality standards.
• Ability to successfully implement quality assurance processes and balance multiple tasks efficiently.

This role offers an outstanding opportunity to contribute to our ambitious projects and collaborate with a team of dedicated professionals. Join us and play a crucial part in our continued success story!

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.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.