Jerome Daquioag Email & Phone Number

Carlsbad, California, United States

• Perform routine inspection and analytical testing to release and support conformity of raw materials and final goods
• Dispositions in-process production by confirming specifications on controlled inspection records
• Facilitates the initiation of nonconformance reports associated with production lots
• Supports material adjustment process for various team’s requests to transfer RUO or specific project materials into inventory
• Follows GMP and GDP protocol according to company quality standard
• Coordinates with supply chain and supplier quality to ensure timely release of reagents consistent with purchase order shipping schedules and customer demands

Carlsbad, California

• Lead team in test procedures and various projects. Confers with supervisor, manager, and director to conduct analyses and interpret test results. Adheres to ISO 13485 and FDA 21 CFR 820 protocol.
• Trained new personnel with regard to technical and operational procedures, SOP’s, and GMP/FDA guidelines
• Performed Design and Development Changes (DDCR), Non-conformance Material Reports (NCMR’s) and Corrective/Preventive Actions (CAPA’s) for individual cohort
• QC representative of company’s safety committee to promote safety awareness

Carlsbad, CA

• Prepares test solutions and reagents for use by laboratory personnel in conducting tests
• Perform Western Blot strip assay test and ELISA
• Perform QC tests on Point of Care (POC) kits via rapid immunoassay testing
• Conduct routine tests on kit components/reagents and College of American Pathologist (CAP) surveys for shelf life, stability, and proficiency
• Familiar and follow SOP's under GMP/FDA regulated working conditions
• Execute Design and Development changes (DDCR) by revising SOP's and batch records

San Diego

• Develop, validate, and update on-line chemometric models for online/at-line LC ethanol processes
• Monitor and evaluate functionality and continuous process control of fermentation spectrometers
• Assist in the delivery of process analytics objectives with cross functional project teams across the BP Biofuels technology organization (San Diego, Jennings, Brazil)
• Conducted tests on process samples for identification and quantification of compounds using spectroscopy and chromatography instruments, such as Vertex nIR/mIR, FOSS XDS nIR, Alpha FT-IR, HPLC, and TECAN,
• Software utilization in: OPUS, OPUS-Lab, Agilent Open Lab, LIMS-link

Greater San Diego Area

• Performed data accessioning on human urine samples and recorded clinical records
• Operated CV1000 automated aliquotter machine for aliquotting batches of samples
• Prepared, aliquotted, and separated batches of drug urine samples prior to analysis
• Stocked supplies, recorded inventory, cupped and uncapped vials, and washed glassware