Michael LeSaar

Seasoned Quality Assurance / Quality Control Leader including cGMP with a Specialty in Documentation, as well as Former Military Information Technology and Services Professional.

Chandler, Arizona, United States

About

Specialties: Experienced with proprietary software for data entry/retrieval and updating/maintaining customer data. Skilled in customer service and telephone operations, handling inquiries, and making presentations in a professional manner. Superior background in assembling products and printed materials. Hard working team player with excellent communication abilities and organizational skills. Computer software skills include: Microsoft Windows, Microsoft Office Suite, and Internet Explorer. I am a former Sergeant in the United States Army where I specialized in line of sight communications for eight years. I lead other soldiers, operated voice and data communication equipment, and deployed mobile communication units while in a combat zone.

Experience

  • Security Guard – U.S. Embassy at VxL Switzerland AG
    Mar 2025 - Jun 2025 · 4 mos

  • Electrical Quality Control (QC) Inspector – Contractor at Xylem Italia
    Feb 2025 - Jun 2025 · 5 mos

  • Delivery Driver at Quickmail AG
    Jan 2025 - Jun 2025 · 6 mos

    ● Executed daily parcel and mail deliveries across assigned routes with precision, timeliness, and customer service focus. ● Managed loading and unloading of packages, ensuring secure transport and accurate sorting by destination. ● Maintained detailed delivery logs, reported route deviations, and communicated effectively with dispatch and logistics teams.

  • Relocation at Career Break
    Jan 2023 - Dec 2024 · 2 yrs

    Acclimating Family To Life In Switzerland (Hausmann)

  • Quality Assurance Specialist (Document Control) at Fine Living Pharmanaturals
    May 2022 - Jan 2023 · 9 mos

    *Responsible for assisting with development, monitoring , and continuous improvement of the quality control systems. * Assist operations and local quality function in tracking, documenting, and reporting. * Review and approval of Master Manufacturing Records. * Create and verify batch record documentation. After fulfilment, review for completeness and accuracy securing corrections when necessary. * Monitor and audit production activities for conformance to cGMP and company policies.