Carlos Quispe

Data Quality Specialist

Raleigh-Durham-Chapel Hill Area

About

Chemist and data‑driven analyst with experience across laboratory method development, machine learning, and AI‑assisted data quality workflows. My background spans analytical chemistry (UPLC/MS, HPLC, GC, NMR), GMP/ICH environments, and computational tools such as Python, SVMs, CNNs, Jupyter, and Azure for scientific and technical analysis. In recent years, I expanded into data governance and structured analytics through the development of the website Rise & Fall of Brands. This project integrates data profiling, anomaly detection, metadata documentation, and AI‑supported cataloging to organize multi‑category datasets (smartphones, TVs, audio, automotive). It strengthened my skills in data quality, content pipelines, and cross‑domain analysis. My earlier work includes method development and validation for APIs, chromatography performance evaluation at Waters Corporation, and QC/QA roles in regulated pharmaceutical environments. I enjoy combining scientific rigor with modern data practices to build reliable systems, improve clarity, and support better decision‑making

Experience

  • Data Quality Specialist at Nova Pharma Tech
    Jul 2025 - Present · 1 yr 1 mo

    Data‑quality and metadata management across scientific and consumer‑brand datasets, applying AI‑assisted workflows (Copilot, ChatGPT, Gemini) to improve accuracy, consistency, and governance. Implement profiling, validation, anomaly detection, and cleansing processes for structured and unstructured sources. Develop lightweight data catalogs and lineage documentation to support analytics pipelines and structured content systems. Integrate scientific rigor from chromatography and GMP environments into modern data quality practices, ensuring audit‑ready datasets and reliable decision‑making frameworks.

  • Data Reviewer Auditor at Cosette Pharmaceuticals, Inc.
    Apr 2024 - Sep 2025 · 1 yr 6 mos

    Verification of documents, reports, forms generated by analysts and scientists in the laboratory are according to cGMP, regulatory agencies requirements and internal SOPs. Compilation of data from stability program testing and protocol driven studies. Use of Empower, Veeva Vault, and Microsoft 365

  • Data Reviewer Auditor at Pfizer
    Aug 2023 - 2024 · 6 mos

    Review analytical data for accuracy, conformance to procedures and specifications, data integrity, and proper documentation in accordance with SOPs and cGMPs. Understanding experiments and assays with continuously update of knowledge of instrumentation and software applications. Use of LabVantage LIMS data management quality system. Microsoft 365

  • Scientist II at GSK
    Dec 2021 - 2022 · 2 mos

  • Technical Support Engineer at PerkinElmer, Inc.
    Nov 2020 - May 2021 · 7 mos

    HPLC and UPLC calibration, Performance Qualification and Instrument Qualification. Trouble-shooting instruments used for Merck pharmaceutical products following GMP and quality systems. SAP Enterprise Resource Planning software