Analytical Section Supervisor (LAB RSCH SUPV 2)

Job Summary

Under general direction of the Laboratory Manager, responsible for monitoring and directing the daily activities of the drug testing laboratory personnel and activities to meet production goals and ensure adherence to internal processes and procedures. As a group leader, directly responsible for assignment and coordination of a wide range of test technologies including screening and confirmation analysis using GC-MS and LC-MS. Responsible for the supervision of multiple chemists and staff performing complex analytical testing procedures. Directs research projects for the analysis of small and large molecules in biological matrices. Responsibilities will involve all aspects of research projects including formulating strategies for novel and new extraction and analytical techniques utilizing LC-MS and GC-MS, supervising personnel, researching literature, and summarizing data for publication. Responsible for direct method development work to enhance the drug testing capability of the lab utilizing new technology as available and participating in the update and development of analytical procedures, quality control procedures, and Standard Operating Procedures (SOPs). Responsible for coordination and planning of confirmation analyses including “B” samples to confirm work of other laboratories.

Responsibilities

• 55% - Lab Management & Supervision
• 25% - Analytical Procedure & Testing/ Quality Program & Other Duties
• 20% - Method Development & Project Assistance

Qualifications

• Advanced degree in Analytical Chemistry, Biochemistry, Pharmacology or a closely related field, or equivalent experience/training with demonstrated experience in related field.
• Experience providing effective management and leadership in a fast-paced, high throughput regulated laboratory environment with strict turnaround times.
• At least 5 years of hands-on experience operating and maintaining LC-MS or LC-MS/MS instrumentation in a laboratory setting and demonstrated ability to troubleshoot complex instrumentation issues independently including skills to quickly evaluate complex issues and identify resolution.
• Experience with LC-MS method development and validation in a regulatory or diagnostic lab environment including proven ability to develop and validate complex methods (including sample prep and analysis) for chromatographic separations with mass spectrometry detection, with strong knowledge of statistics and QA/QC principles to ensure accuracy and robustness.
• Strong organizational skills, independent thinking, and problem-solving skills with the ability to prioritize and manage multiple tasks/projects and deliver high-quality results including skills to obtain, comprehend, and consider others’ priorities, opinions and concerns.
• Demonstrated success in leading, motivating, and mentoring multidisciplinary teams in a collaborative environment.
• Familiarity with ISO, or other regulatory frameworks relevant to analytical testing.

Preferred Qualifications

• Master’s degree in Analytical Chemistry, Biochemistry, Pharmacology, or a closely related field, or equivalent experience/training including membership in the Association of Official Racing Chemists.
• Extensive supervisory/management experience in a laboratory environment including performance management, coaching, hiring/releasing staff, and directing the work of others.
• Extensive knowledge of instrument maintenance, calibration, and performance optimization for Thermo LC-MS and Agilent GC-MS systems including data analysis software. (Q-Exactive, Quantiva, Altis/Tracefinder, Xcalibur, Masshunter).