Role Summary
This opportunity is designed to help you grow your career and contribute to scientific innovations that have a positive impact on patients' lives.
The successful candidate will be responsible for planning, coordinating, and executing all quality control (QC) required sections for annual product quality review (APQR) reports. Additionally, they will define, schedule, coordinate, and drive to completion all annual trend reports.
The ideal candidate should possess a BSc in Biochemistry or a related field, as well as at least three years of hands-on experience working in a Good Manufacturing Practice (GMP) laboratory setting. Prior experience with QC trending, preferably in biologics, is also highly desirable.
The technical requirements include expertise in high-performance liquid chromatography (HPLC), ultra-performance liquid chromatography (UPLC), capillary electrophoresis (CE), capillary isoelectric focusing (cIEF), sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), Biacore, bioassay, and compendial techniques such as kinetic flocculation (KF) and high-ionic-strength agar column (HIAC).