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Screening Supervisor

Davis

UC Davis Screening Supervisor Salary or Pay Range: $77,100/yr. - $139,900/yr. – Please note this position is subject to a departmental budgeted salary range of: $77,100/yr. - $105,300/yr., commensurate with educational background and relevant work experience. 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 analysis using GC-MS, LC-MS, and immunoassay analysis. Responsible for the supervision of multiple chemists and staff performing complex analytical testing procedures. Under general guidance from the laboratory manager and in conjunction with graduate students and academic personnel, direct 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). Minimum Qualifications - For full consideration, applicants are encouraged to upload license and/or certification if required of the position • Required to hold a valid California driver's license, have a driving record that is in accordance with local policies/procedures, and/or enroll in the California Employer Pull Notice Program • Advanced degree in Analytical Chemistry, Biochemistry, Pharmacology or a closely related field, or equivalent experience/training with demonstrated experience or 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. Demonstrated ability to troubleshoot complex instrumentation issues independently. Skills to quickly evaluate complex issues and identify resolution. • Experience with LC-MS method development and validation in a regulatory or diagnostic lab environment. 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. • 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). Key Responsibilities • 55% - Lab Management & Supervision • 20% - Analytical Procedure & Testing • 20% - Method Development 7 Project Assistance • 5% - Quality Program & Other Duties Special Requirements – Please contact your recruiter with questions regarding which activities apply by position • This is a critical position, as defined by UC Policy and local procedures, and as such, employment is contingent upon clearing a criminal background check(s) and may include drug screening, medical evaluation clearance and functional capacity assessment To view full job description and submit an on-line application, visit UC Davis Career Opportunities at: http://50.73.55.13/counter.php?id=308979 Job ID#: 80940 The University of California, Davis is an Affirmative Action/Equal Opportunity Employer