Landri S.

About Landri S.

As a Manufacturing Specialist, I safeguard patient safety and product quality by identifying true root causes, developing effective CAPAs, and leading investigations ranging from minor to major severity. I collaborate closely across manufacturing, QA, QC, engineering, and support teams to ensure issues are fully understood, addressed, and prevented from recurring. My work is driven by a commitment to compliance, strong scientific reasoning, and clear cross‑functional communication.Before transitioning into quality investigations, I spent over 3 years as a Research & Development Process Scientist, specializing in downstream protein purification, process optimization, analytical problem‑solving, and data visualization. I leveraged these skills to improve small‑scale purification workflows within influenza vaccine development, strengthening process robustness and supporting reliable biologics production.

Experience

1. Manufacturing Specialist Ii

   CSL

   Mar 2025 — Present · Raleigh-Durham-Chapel Hill, NC, US

   Investigate Bulk Manufacturing deviations from Virus Seed, Support, Upstream, and Downstream value streams-Utilize Root Cause Analysis Tools (RCA) to determine true root cause-Develop Corrective Action/Preventative Actions (CAPA) and Effectiveness Checks (EC)-Collaborate and coordinate with cross-functional groups (MS & T, Engineering, QC, Maintenance, Sterility)-Reconcile with Quality Assurance (QA) to uphold product specifications and regulatory standards

Education

• University of North Carolina Wilmington

  Bachelor of Science - BS, Biology, General Minor in Chemistry