Robert di Lonardo

Vice President, Global Quality Assurance@Alira Health
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Summary

Championing Compliance, Quality Culture & Innovation in Life Sciences to Humanize Healthcare as Vice President of Global Quality Assurance & Compliance at Alira Health | MSc Regulatory Affairs. Quality Assurance professional with 20 years of experience in the regulated pharmaceutical and medical device industry. I hold an M.Sc. in Regulatory Affairs and a B.Sc. in Anatomy and Cell Biology, providing a strong foundation in life sciences and regulatory compliance. My expertise spans the drug development lifecycle (GLP, GMP, GCP) and Software as a Medical Device (SaMD) development, ensuring compliance and quality excellence. As a dedicated member of QA professional associations (SQA, RQA, RAPS), I make it a priority to stay informed on the latest industry trends, best practices, and regulatory updates. This proactive approach allows me to remain ahead in my field, equipped with the knowledge and skills necessary to excel in my role and contribute effectively to the success of my team and organization.

Work experience

  • Vice President, Global Quality Assurance

    Alira Health
    2025.01-Current(2 years)
  • Senior Director, Global Quality Assurance

    Alira Health
    2024.04-2025.02(a year)
  • Northeastern University Experiential Network Project - Regulatory Strategy

    Provista AI
    2024.04-2024.06(3 months)
  • Director, Global Quality Assurance & Compliance - Digital Health/Clinical Operations

    Alira Health
    2022.05-2024.04(2 years)
  • Compliance Specialist

    RI-MUHC | Research Institute of the MUHC | #rimuhc
    2021.05-2022.05(a year)
  • Quality Assurance Manager

    Certara
    2020.04-2021.05(a year)
  • Senior Quality Assurance Specialist

    Certara
    2018.03-2020.04(2 years)
  • Consultant and Founder

    Quality Advice Consulting Services Inc.
    2016.01-2018.03(2 years)
  • Validation and Metrology, Quality Operations

    Pfizer
    2018.01-2018.01
  • Senior Quality Assurance Manager

    Montreal Pharmacokinetics Inc.
    2017.01-2018.01(a year)
  • Senior Specialist, Global Computer Validation QA

    Charles River Laboratories
    2012.04-2016.12(5 years)
  • Project Manager

    Charles River Laboratories
    2011.03-2012.04(a year)
  • Quality Systems

    GSK
    2010.01-2011.01(a year)
  • Principal Inspector, Quality Assurance

    Charles River Laboratories
    2008.08-2010.12(2 years)
  • Senior Inspector

    Charles River Laboratories
    2008.02-2008.08(7 months)
  • Inspector, Quality Assurance

    Charles River Laboratories
    2006.02-2008.02(2 years)

Educational experience

  • Northeastern University

    Master of Science - MS, Regulatory Affairs - Quality Assurance and Compliance, 3.95
    2021.01-2024.01(3 years)
  • McGill University

    BSc, Anatomy and Cell Biology Major, Management Minor
    2002.01-2005.01(3 years)
  • Vanier College

    DEC, Health Science
    1998.01-2001.01(3 years)
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