Elisabeth Landing

Elisabeth Landing

Laboratory Assistant

Followers of Elisabeth Landing381 followers
location of Elisabeth LandingBristol, Tennessee, United States

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  • Timeline

  • About me

    Director, Quality Systems and Compliance | GMP | GCP | GLP | GDPR | Vendor Management | Metrics | Quality Agreements | Validation | Electronic Quality Systems Management | Drug Development & Manufacturing

  • Education

    • University of Maryland, Baltimore County

      2009 - 2011
      Graduate Certificate Biochemical Regulatory Engineering
    • Towson University

      1998 - 2002
      B.S. Biology

      Minor: Chemistry

    • University of Maryland Baltimore County

      2009 - 2011
      M.S. Engineering Management
  • Experience

    • Towson University

      Sept 1998 - May 2002
      Laboratory Assistant
    • Celsis In Vitro Technologies Inc.

      Nov 2001 - May 2004
      Associate Scientist

      In my role as an Associate Scientist at Celsis In Vitro Technologies Inc., I performed tissue and cell culture for metabolism studies, executed drug metabolism studies, and trained in Biological Safety Level 2 laboratory procedures. My work contributed to advancing research in drug metabolism and cell culture assays.

    • Shire Pharmaceuticals

      Jun 2004 - Nov 2011

      In my role as a Sr. Quality Engineer at Shire Pharmaceuticals in Owings Mills, MD, I analyzed quality and facility key performance indicators, approved quality investigations, and supported SAP as a quality management master administrator. I also participated in quality and process improvement initiatives, ensuring cGMP compliance and safety in product operations.

      • Sr. Quality Engineer

        Oct 2006 - Nov 2011
      • Quality Assurance Technician I, II

        Jun 2004 - Sept 2006
    • UPM Pharmaceuticals, Inc.

      Dec 2011 - May 2021

      In my role as Quality Assurance Director at UPM Pharmaceuticals, Inc., I provided strategic leadership in quality management activities, ensuring compliance with industry regulations and standards. I oversaw all aspects of the quality unit, including product complaint program, internal audits, and supplier quality program. My efforts in implementing change control processes led to improved efficiency and compliance within the organization.

      • Director, Quality Systems and Compliance

        Jul 2014 - May 2021
      • Site Head, Quality Assurance

        Oct 2012 - Jun 2014
      • Associate Quality Assurance

        Dec 2011 - Sept 2012
    • Landos Biopharma, Inc. (acquired by AbbVie)

      Jun 2021 - Sept 2024
      Director, Quality Systems

      In my role as Director of Quality Systems at Landos Biopharma, Inc., I spearheaded the development and implementation of robust quality management systems. By managing vendor relationships, conducting audits, and overseeing deviations, I ensured the highest standards of quality were maintained. Through training initiatives, I enhanced the team's capabilities and fostered a culture of continuous improvement.

    • Avidity Biosciences, Inc.

      Dec 2024 - now
      Director, Quality Systems & Compliance
  • Licenses & Certifications

    • GCP for Clinical Trials with Investigational Drugs and Biologics (ICH Focus)

      CITI Program
      Aug 2023
      View certificate certificate
    • Good Manufacturing Practices (GMP)

      CITI Program
      Jun 2023
      View certificate certificate
    • FDA Inspections: From Site Preparation to Response

      CITI Program
      May 2023
      View certificate certificate