David Oveysey
Sims,NC
Summary
A recent graduate from East Carolina University's Thomas Harriot College of Arts & Sciences, Department of Biological Science & Technology, with a Bachelor of Science in Molecular Biology. My studies focused on Biological Science, specifically Microbiology, Biochemistry, and Chemistry. During my time at Pfizer Pharmaceutical Inc. in Rocky Mount, NC from February 2022 to October 2024, I gained valuable experience in upgrading, monitoring, and research using the Scientific Method. I also developed strong teamwork and communication skills. I am dedicated to excellence and have demonstrated leadership as both an employee and student. Proficient in applying Scientific Models in Biology, Biochemistry, Chemistry, and performing various Quality Control tasks. Skilled in Diagnostic, Contamination, Instrumentation, Calibration, Analyzing Samples, protein purification, Titration, Dissolution, Automation, Filtration, Reactivity, HPLC, GC, spectroscopy UV-Vis, FTIR, NIR, IR, AA/AE, and NMR. Experienced in collecting and recording reports of incoming Test Samples for various Analytes. With my knowledge and experiences combined with my credentials, I am a well-qualified candidate for the designated position. I am eager to join your scientific team as a loyal and hard-working member who prioritizes the company's goals.
Overview
3
3
years of professional experience
1
1
Certification
Work History
Chemist I
Pfizer Pharmaceutical Inc.
02.2022 - 10.2024
- I was a full-time chemist employee at Pfizer Pharmaceutical Inc., Rocky Mount, NC from February2022 to October2024 and have been trained and certified internally at Pfizer Inc., in all duties as assigned to the position that I had
- Specialized and experienced with ability to successfully perform the duties of the assigned position and related skills
- Ability to work within a team environment and interface with peers, management, etc
- Self-motivated with strong organization skills following written procedures along high level of attention to details and ability to work independently, handle multi-tasks simultaneously across project and activities with minimal direction and adhered consistently to the site cGMP, GLP, FDA, DEA, SOPs, and Manufacturing safety procedures
- Developed collaborative relationships with staff in each of business units and the appropriate quality representatives to facilitate continuous improvement of applicable areas, and adhered and worked within a team environment and interface with peers, management, etc
- Knowledge of analytical organic and inorganic chemical quality laboratory procedure inclusively wet chemistry, chromatography, HPLC, GC, Karl Fisher titration, dissolution, reactivity, pH and density measurements, buffer preparation, ultra-filtration, spectroscopy, UV-Vis, FTIR
- NIR, IR, AA/AE techniques adhering with cGMP/GLP requirements, ICH, FDA, USP and other pharmaceutical industry standards when implemented
- Performed manufacturing protocols, helped resolve deviation/discrepancies, analyzes study data, and write summery reports and provide solutions to routine technical problems of limited scope and support the resolution of regulatory observations of manufacturing site issues, risk analysis, and data integrity assessment
- Performed product characterization/analysis tests and techniques (viscosity, particle size analysis, pH and density measurements, etc.) and analyzing, planning, execution of test methods and application of instruments
- Performed routine laboratory testing within equipment validation IQ, OQ, PQ manufacturing equipment in adherence with DEA, FDA, cGMP, GLP, and SOP’s manufacturing policies and high-quality standards.
- Knowledge of EM/BQ and Diagnostics Laboratory procedures gram stain, microbial identification, biochemical testing, pipetting, DNA isolation and sequencing and maintaining data in gLIMS and pertaining with laboratory logbooks among providing an efficient focused service, ensured laboratory processes and equipment and services are maintained in a standard operational state, as well as aseptic technique, classified area, Isolator interventions, Aseptic gowning, and necessary assessments of aseptic and Terminal Sterilized SVP injectable/filling product and update necessary documents as well as viable and non-viable monitoring of the manufacturing areas, including air, water, and surface, rinse, and swab sampling recovery as well as operation, maintenance, troubleshooting, and calibration of laboratory equipment
- Trained and certified by Pfizer on Job Aid Control Substance, Chemical Quality and Biological Quality Laboratory, Control Substance & API security & Handling, Foreign Material Discovery, identification, Investigation initiation, Biosafety Assay, DIIA, cGMP, CMMS GMP, gLIMS, MODA, GLP, GXP, APEX-ENT, CQ Scientific Report etc
- Demonstrated successful hands-on analytical testing experience in a cGMP environment and strong organizational skills and ability to multi-task across projects and activities
- Ability to ensure reports are aligned to regulatory compliance requirements and company policies along with timely documentation and resolution of events
- Developed working process to ensure enhanced manufacturing (cGMP) along Standard Operating Procedure and continuous improvement projects
- Reviewed (QC), (GXP) of all results in accordance with (GDP), (GLP), (GXP) and Manufacturing Quality Standards, ensuring compliance with all policies and procedures are in accordance with SOPs, and Handbook requirements
- Demonstrated proficiency in computerized system such as MS Word, Excel, PowerPoint, MODA, gLIMS, EAMS, and Track Wise
Education
Bachelor of Biological Science - Molecular Cell Biology
East Carolina University
Greenville, NC01.2020
Skills
- Excellent scientific analytical problem solving
- Bioinformatic screening, NDNAD, NCBI-RefSeq, GenBank, NIH, Swiss-Prot, Uniprot
- Affymetrix microarray, cDNA & RNA, NGS sequencing, SDS-PAGE, Northern Blot, Southern Blot, BLAST, ELISA
- Genomic sequencing NGS, WTSS DNA extraction, qPCR, PCR, Gel electrophoresis, & fluorescent emission properties
- Quality Control of Biological and Microbiological Aseptic technique, identification & assay analysis and DNA sequencing and QC laboratory, SOP, GCP, cGLP, cGMP, GDP, aseptic procedure, sterilization, calibration, endotoxin, cell culture, Inoculation, Incubation, Morphology, Gram Stainer, Microscopy, Gene identification (Bacteria & Fungi) MIDI, VITEK, Biolog, and Bioprinter
- Environmental Monitoring, Terminal Sanitation, Aseptic process simulation, Manufacturing Area Monitoring, Air, Water, Surface, Rinse, Swab sampling
- Bioanalysis gLIMS & interpretation of Scientific Laboratory Data
- Biochemistry & computational laboratory skill, protein purification, column chromatography
- Organic & Inorganic synthetic techniques & analytical chemistry, ion chromatography, HPLC, GC, titration, dissolution, wet chemistry, pH, reactivity, test analytes, Buffer preparation & Ultra-filtration, Spectroscopy HNMR, UV/Vis, FTIR, NIR/IR, and NMR
- Pharmaceutical compound screening, Random & HTS
- Microsoft Office, Word, Excel, PowerPoint, gLIMS, MODA, and Track Wise
Certification
- Certified Microsoft Network System Engineering.
- Certified CompTIA computer Service Technician # D12DTT3124.
Academic Professional Experience
- Research clinical study on reginal enhanced expression of HOX gene family of HOXA5 short RNA on A549 lung cancer, colorectal cells cancer of HC116, DLD1, & HT29 among normal colonic epithelial cells of HCEC-1CT.
- Studied two years of organic and inorganic chemistry and biochemistry and assigned laboratory curriculums.
- Performed research clinical laboratory practice and study of eukaryote cell proliferation of Telomeres Terminal Transferase Activity, undergoing senescence.
- Performed genetic sequence per protein purification for biochemical activities of the target cells.
- Performed microbial identifications via Chromogenic Media, Microscopy, Biochemical testing and Molecular techniques.
- Performed two years of laboratory microbial identification of fungi and bacterial organisms based on environmental isolation using DNA sequencing to identify the genus and species level relevant to biological quality and biochemistry (Catalase and Coagulase) of those target species’ vital process and internal procedure.
Languages
English
Professional Working
Timeline
Chemist I
Pfizer Pharmaceutical Inc.
02.2022 - 10.2024
- Certified Microsoft Network System Engineering.
- Certified CompTIA computer Service Technician # D12DTT3124.
Bachelor of Biological Science - Molecular Cell Biology
East Carolina University
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