- Draft and execute change controls for qualified/validated processes, systems, and equipment.- Author and revise Standard Operating Procedures (SOP) in accordance with cGxP requirements andPfizer policies while working with supporting groups to meet team and departmental deadlines.- Performed sample preparation for preclinical and clinical serum/urine based assays to supportvaccine development and clinical studies. This includes manual and robotic sample preparation, useand… Show more - Draft and execute change controls for qualified/validated processes, systems, and equipment.- Author and revise Standard Operating Procedures (SOP) in accordance with cGxP requirements andPfizer policies while working with supporting groups to meet team and departmental deadlines.- Performed sample preparation for preclinical and clinical serum/urine based assays to supportvaccine development and clinical studies. This includes manual and robotic sample preparation, useand maintenance of appropriate equipment, and preparation of relevant reagents. Show less

- Assist GMP officers and QA operations through the transfer, organization, and release of patient batch record information- Track incoming patient samples to issue the appropriate batch record and sample media forms to ensure that orders are executed and sent back on time to the requesting physician

- Explored the viability of Moorella Thermoacetica as a means of carbon capture by converting carbon emissions to acetic acid and other useful compounds under the proper conditions- Grew yeast cultures to practice proper aseptic technique and analyzed cell concentration curves by means of a spectrophotometer and the Lambert – Beer Law to calculate doubling time and observe how changing certain parameters affected this

- Routine inspections of vessels, piping, and safety critical equipment around the plant to document necessary repairs and safety hazards- Supervised and worked with outside contractors and plant maintenance to complete jobs safely and correctly- Analyzed P&ID’s to ensure safety critical initiatives are met and equipment designations are made accurately

- Assisted lead scientist with SDS page and western blot analysis to identify the qualitative presence and transfection efficiency of proteins and antibodies of interest from the host cell culture - Conducted protein structural analysis in support of protein manufacturing process development to determine molecular weight, structure, and purity to investigate the efficiency of different purification processes - Prepared specific buffer solutions based on what protein purification… Show more - Assisted lead scientist with SDS page and western blot analysis to identify the qualitative presence and transfection efficiency of proteins and antibodies of interest from the host cell culture - Conducted protein structural analysis in support of protein manufacturing process development to determine molecular weight, structure, and purity to investigate the efficiency of different purification processes - Prepared specific buffer solutions based on what protein purification process was being conducted from day to day Show less