QCL Management Team
Formulations & Manufacturing Development Director
Emily has a PhD in Pharmaceutical and Biomedical Sciences and a background in Chemical Engineering. She joined QCL in 2020 with a wide variety of experience from 18 years in the pharmaceutical industry including formulation development, taste-masking, technology transfer and scale-up, pre-formulation characterization, lean six sigma, computer system validation, and expertise in implementing electronic laboratory notebooks with instrument integration. Specializing in oral liquid and solid dosage forms, Emily has experience in high-shear granulation, fluid-bed granulation, roller compaction, milling, blending, tableting, encapsulation, liquid-filled hard-gelatin capsules, capsule banding, Wurster coating, and perforated pan coating technologies. She is the director of QCL’s formulation and manufacturing development team.
Ruth McKnight, ASQ, CQA
Quality Assurance Director
Ruth has been a member of the Quality Chemical Laboratories team for 15 years. She is responsible for hosting customer audits, regulatory inspections, and has oversight of cGMP compliance company-wide.
Manufacturing QA Director
Tony has 28 years in the pharmaceutical industry and joined QCL in 2020. He is responsible for Quality oversight of Formulations and cGMP manufacturing.
Mark has over 20 years of experience in the pharmaceutical and chemical instrumentation industry, including 7 at QCL. He manages the metrology department ensuring our instrumentation maintains the highest levels of precision, accuracy, and reliability.
IT & Infrastructure Manager
Kenner has 24 years in the pharmaceutical industry and joined QCL in 2012. He is responsible for company-wide Information Technology and Infrastructure in in QCL’s data-driven business of science.
Biotechnology Lab Manager
Audrey entered the industry in 2003 and joined QCL in 2018 to establish our presence in the Biotechnology arena. She is experienced in the genomics and proteomics field with a focus on gene expression, post-translational modifications, DNA and RNA sequencing, and real-time PCR. Audrey’s emphasis has been on protein and enzymatic assays, cell-based assays, residual DNA testing, Microflow Imaging (MFI), and SDS-PAGE.
Gina Holliman, Manager
Raw Material Labs & Sample Log-in Group
Gina has been in the pharmaceutical industry for 16 years and with QCL the last 8 years. She manages the first shift of our Raw Material/Wet Chemistry labs and the Sample Log-in department