**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.
