QA Specialist III-Operations OTF (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.

Join Lonza AG as a QA Specialist III-Operations OTF and play a crucial role in maintaining our extraordinary operational processes that adhere to GMP standard! This position in New Hampshire, USA, offers an outstanding chance to create a direct impact on our ambitious growth trajectory.

Key responsibilities:

• Perform daily rotations through GMP operational areas, ensuring flawless review of GMP documentation and observation of work habits.

• Provide outstanding mentorship and feedback on documentation behaviors, collaborating closely with Manufacturing Management.

• Provide proven GMP mentorship on routine and non-routine issues, elevating sophisticated matters to senior staff and Management as needed.

• Respond promptly to QA Hotline calls, effectively supporting GMP operations.

• Independently make simple GMP decisions while collaborating with senior staff or management for sophisticated decision-making.

• Authorize placement and removal of Quality Tag Outs, and release equipment from Product Changeover.

• Apply Data Integrity principles in all aspects of work, ensuring compliance with Lonza's DI policies, guidelines, and procedures.

• Represent QA in meetings or project teams, learning to successfully implement decisions as a QA representative in collaboration with senior staff.

Key requirements:

• Bachelor's Degree or equivalent experience required.

• 5-10 years of experience in a related field.

• Outstanding attention to detail and a dedication to maintaining high standards of quality and compliance.

• Ability to work independently and as part of a collaborative team.

• Strong problem-solving skills and the ability to successfully implement solutions in a fast-paced environment.

• Excellent communication skills, both written and verbal.

• Confirmed experience in a GMP environment, with an extensive understanding of GMP principles and practices.

Join Lonza AG and help us continue to compete at the highest level while making a meaningful difference in the world.

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.