US02 Lonza Biologics Inc.
QA Compliance Project Manager, Quality Systems (Biotech)
The QA Project Manager, Quality Systems is assigned as the primary liaison to internal customer(s) for all quality-related items including temporary and permanent change controls, deviations, standalone investigations, and CAPAs. Responsible to facilitate discussions between internal groups such as MSAT, Manufacturing, Engineering and QC. For these quality-related items, the Project Manager coordinates the process for owning the quality systems for Deviation, Change Control and CAPAs. Responsibilities include oversight of the system process, training, metrics, and hosting meetings (Deviation Review Board, CAPA Review Board, and Change Control Committee).
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.