Lonza Inc.
QA Specialist IV-QRM (Biotech)
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.
Are you ready to be part of a world-class team at the forefront of life sciences? Lonza AG is seeking an exceptionally dedicated QA Specialist IV-QRM to join our ambitious team in New Hampshire, USA! This role is critical in ensuring compliance with cGMP regulations related to quality systems, specifically through our Quality Risk Management (QRM) program. As we continue to grow and innovate, your work ethic will help us maintain our flawless standards and successfully implement effective quality systems.
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.