On-site Management responsible for all Toxicological work in the laboratory. - Directly responsible for validation of new equipment allowing for doubling of sample growth within a 6 month period(2,000 to 4,000 samples monthly) without sacrifice of meeting expected Turn Around Time and Quality standards, helping to drive increased business profitability. • Provided all on-site supervision of all department testing personnel during day-to-day operations. • Distributed work and performed employee assessments with special attention to encouraging personnel growth while ensuring adequate employee engagement. • Performed advanced/specialized tests and related laboratory technique including screening via Immunoassay and preparation of toxicological specimens for testing in both blood and hair. • Evaluated testing methodologies, recommended changes and assisted in test interpretation.

Directed all work in the Toxicology section of the laboratory with an emphasis to maximize employee, equipment and material utilization while adhering to established quality technical standards in a high complexity (LC-MS/MS) clinical laboratory environment. Main point of contact in developing and validating testing methods, organizing and developing laboratory layout and directed all processes involved in starting up a new clinical toxicology laboratory.- Provided direct on-site supervision of all department testing personnel during day-to-day operations. Distributed and assigned work, performed personnel related function(hiring, training, etc.)- Performed advanced/specialized tests and related laboratory technique. Evaluated testing methodologies, recommended changes and assisted in test interpretation.- Checked and approved all specialized and problem reports for accuracy.- Initiating quality control measures and monitored quality of work for adherence to laboratory standards.- Completed special projects as requested, including but not limited to: CAP surveys, statistical reports, method development and validation for LC-MS systems

Performed complex testing of raw materials and finished products in compliance with cGMP protocols (USP, EP and JP) and procedures for multi-national pharmaceutical production company. Participated in troubleshooting calibration and maintenance for instruments as required. Followed SOPs while maintaining adherence to protocols ensuring integrity of data. • Participated in analytical method validation for intermediate precision studies involving testing of raw materials, APIs, finished products, stability, and cleaning verification samples. • Routinely performed peer review of analytical documentation and adherence to safety protocols. • Demonstrated proficiency and performed sample analysis using multiple testing methods including pH, viscosity, osmolality, HPLC, GC, FTIR, AA, Karl Fischer, and UV/Vis spectroscopy. • Utilized engineering skills (DMAIC Green Belt, kt Problem solving) to improve testing and reporting efficiencies by identifying non-value added steps as well as elimination of redundancies when possible.

Solved process issues through data analysis, experimentation, and implementation of engineering methodologies. Provided engineering-level production and supervision support to manufacturing operations. Helped to execute cost reduction strategies and to implement LEAN strategies to improve current production and drive continuous improvement. • Helped to streamline current processes and identify means of improvement. Developed troubleshooting strategies for ICP-OES as well as XRF and solution preparation safety protocols focused on proper chemical technique highlighting employee safety. • Utilized Six Sigma and kt problem by leading the use of these analysis and decision-making tools to develop sound problem analysis and data driven decision to identify and implement controlled change. • Provided training and leadership to technologist within the glass technology laboratory. Assisted with instrument troubleshooting as well as to document process change to allow for clear and concise operation leading to improved instrument precision and accuracy. • Collaborated with colleagues across functional areas to drive overall process change in line with the needs of the company as well as utilizing technical expertise to ensure proper implementation.

Prepared and interpreted toxicological drug screens for both in and outpatient clinics for the University. Ran multiple instruments to help determine serological outcomes used directly in-patient care to help improve patient health outcomes. • Extensive experience in troubleshooting and interpreting LC-MS/MS work. Participated in LC-MS/MS Research and Development projects to develop new testing methods to bring testing in-house. • Assisted in the development of the interfacing between new and existing instruments with LIMS medical records software to allow for increase in efficiency and accuracy in result screening. • Helped to develop and train newly hired laboratory personnel in proper laboratory testing techniques. • Assisted master lab technologists with multiple development projects including GC-MS and LC-MS/MS optimization as well as serological instrumentation. • Working Proficiency in use of the Abbott Architect, Bio-Rad Varient and Bioplex, Beckman Coulter Access, Agilent GC-MS, Shimadzu and ABSciEx LC-MS/MS and UV-Vis Spectroscopic systems.