Analytical Chemistry Supervisor- 2nd Shift

What We're Looking For The Supervisor, Analytical Chemistry (2nd Shift) is responsible for providing scientific, logistical, and personal leadership within the analytical chemistry team focused on raw material, finished product, and stability testing. This individual will leverage their expertise to ensure the quality and efficiency of all analyses, drive continuous improvement, and expand the laboratory’s capabilities in support of pharmaceutical testing and compliance requirements. This role requires effective management of laboratory operations, personnel, and resources specific to the evening schedule, ensuring seamless transition and communication between shifts. Responsibilities Oversee, schedule and perform routine and non‑routine analytical testing of raw material, finished product, and stability samples according to established procedures and regulatory guidelines; ensures testing is completed within required timelines. Reviews and interprets test results for accuracy and compliance; promptly notifies management of any unexpected or out‑of‑specification results and leads investigations and troubleshooting with minimal supervision. Supervises the maintenance, calibration, and troubleshooting of analytical equipment (e.g., HPLC, GC, FTIR, UV‑Vis Spectrophotometer, TOC analyzer, Wet Chemistry testing equipment) used for raw material, finished product, and stability testing to ensure all instruments are operating within calibration and performance standards; coordinates repair and preventive maintenance activities as needed. Ensures team members maintain proficiency with all relevant equipment, systems, and standard operating procedures (SOPs) specific to raw material, finished product, and stability analysis. Keeps current with advances in analytical techniques, instrumentation, and regulatory expectations for raw material, finished product, and stability testing, with an emphasis on pharmaceutical industry standards. Provides leadership and support across all raw material, finished product, and stability testing workstations, facilitating cross‑training and backup coverage as needed to ensure uninterrupted laboratory operations. Ensures meticulous and compliant documentation of all testing activities, results, and investigations in accordance with cGMP and data integrity requirements. Leads the development, revision, and review of SOPs and laboratory documentation specific to raw material, finished product, and stability testing, ensuring timely updates to align with regulatory and operational changes. Qualifications Bachelor’s, Master’s or Doctorate degree in Analytical Chemistry or related science field, with directly related experience of 3–4 years in an analytical chemistry laboratory within pharmaceutical industry Hands‑on experience with sample preparative chemistry and wet chemistry analysis per compendial monograph procedures Understanding of instrumental analysis procedures utilized in a modern chemistry laboratory Demonstrated competence with computer applications and programs related to laboratory applications Knowledge of sampling methods and quality control systems. Equal Opportunity Employer. This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor. #J-18808-Ljbffr BioSpace