**QC Scientist**
The QC Scientist will be responsible for examining and revising internal documents to align with updates in compendial standards and pharmacopeial guidelines. Additionally, they will coordinate testing with external contract laboratories and manage the entire lifecycle of controlled documents and analytical reports. Applicants should have a Bachelor’s degree in a scientific discipline and bring 3 to 5 years of experience in a regulated pharmaceutical quality control environment. Expertise in analytical techniques, including HPLC, GC, and FTIR, as well as a thorough understanding of global pharmacopeias, is essential.
Lonza provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
