Sr. Coordinator, QA

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 Sr. Coordinator, QA in our dynamic Manufacturing team in Greenwood, SC, USA. This role is crucial in ensuring that our high standards for quality and safety are strictly maintained. As part of our ongoing growth, you will have the opportunity to contribute to our mission of improving lives through science. We value ambitious and collaborative professionals who are ready to deliver world-class results.

• Coordinate all QA activities related to finished product disposition.
• Conduct the final review of batch records to ensure all cGMP requirements are met.
• Coordinate with cross-functional teams to complete batch record reviews, corrections, investigations, and testing by target ship dates.
• Make final disposition decisions and issue Finished Product Certificates of Analysis.
• Perform second reviews and issue printed batch records to Operations for execution.
• Review and approve recipes in the MES system.
• Provide QA MES exception reviews and approvals.
• Conduct daily meetings with Supply Chain, Production, and Quality colleagues to review critical path items required for finished goods release.
• Initiate and coordinate deviation investigation review meetings.
• Assist Process Engineers with manufacturing deviation investigations and final reviews.
• Manage the system for logging, organizing, and storing completed batch records and retain samples.
• Ensure all orders for “month end” are processed and approved timely.
• Support other DFS activities as needed.
• Commit to a minimum of 40 hours a week, including weekends and holidays as required.

• Bachelor's degree in business or a technical field.
• Sophisticated experience in the dietary supplement business or a quality role in another industry.
• Proficiency in MS Office and other relevant software.
• Excellent communication skills, both verbal and written.
• Ability to interact effectively with colleagues at all levels of the business.
• Capable of making timely and sound business decisions.
• Ability to manage work stress and pressure in intense situations.
• ASQ certification preferred.

Apply today to become part of an outstanding team where your ideas can make a genuine impact on the world!

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

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 sophisticated 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.