Quality Control Supervisor - Overnight

Our client is seeking an experienced Overnight Quality Control Supervisor to lead analytical testing operations in a GMP-regulated environment. This role focuses heavily on HPLC/UPLC/GC analysis, method development/validation, team leadership, and regulatory compliance supporting drug product manufacturing. Key Responsibilities Supervise and manage daily QC analytical testing for raw materials, in-process, and finished products Lead and mentor a team of scientists, driving productivity, training, and performance management Oversee HPLC, UPLC, and GC testing, including method development, validation, and troubleshooting Ensure compliance with cGMP, USP, EP, and FDA regulations and maintain accurate laboratory documentation Conduct and support investigations including OOS, deviations, CAPAs, and change controls Coordinate laboratory workloads, timelines, and multiple projects in a fast-paced environment Support pharmaceutical manufacturing through analytical testing and quality oversight Maintain safe laboratory operations and adherence to all safety procedures Qualifications Bachelor’s degree in Chemistry, Analytical Chemistry, or related scientific field 3+ years of experience in a GMP/GLP laboratory environment Strong hands‑on expertise with HPLC, UPLC, GC, method development, and method validation Minimum 2 years of supervisory or team leadership experience Deep knowledge of FDA regulations, cGMPs, USP, and EP requirements Strong communication, organizational, and investigation skills with the ability to manage multiple priorities simultaneously #J-18808-Ljbffr Astrix