Description
The Quality Control Laboratory Manager provides scientific, technical, and operational support to the Quality Control organization and leads the site’s stability program. Responsibilities include managing stability chambers, conducting and reviewing cGMP pharmaceutical testing, developing stability documentation, analyzing trends, investigating OOS/OOT events, supporting method transfers and validations, troubleshooting chromatographic instrumentation, and mentoring analysts. The role requires a bachelor’s degree in a relevant science field and at least eight years of GMP-regulated QC laboratory experience, with pharmaceutical or biotechnology experience preferred. The base salary starts at $120,000, with additional health benefits and a discretionary annual target bonus for full-time positions.
