Maggie Ladd

Senior Principal Consultant at RQM+
  • Claim this Profile
Contact Information
us****@****om
(386) 825-5501
Location
Alpharetta, Georgia, United States, GE

Topline Score

Topline score feature will be out soon.

Bio

Generated by
Topline AI

5.0

/5.0
/ Based on 2 ratings
  • (2)
  • (0)
  • (0)
  • (0)
  • (0)

Filter reviews by:

John Cecilia

I had the opportunity to work with Maggie in the Health Care sector of Kimberly-Clark Corporation. Maggie always exhibited a positive blend of technical knowledge and support along with an ability to work successfuly across all levels of the organization. She demonstrated a good understanding of recognizing the need for excellent customer service while managing a critical aspect of the product supply process.

Julie Ambrose

It's a great honor to recommend Maggie. She is a well qualified scientist with excellent technical skills. While Maggie is also a hard working and thorough project manager, her most valuable strengths lies in her ability to inspire a group to come together around a very challenging goal. She inherited one quality resolution project from me, that required unusual persistence and resilience. Maggie managed the effort with grace and tenacity, and endeared herself to the team at the same time.

You need to have a working account to view this content.
You need to have a working account to view this content.

Credentials

  • Coaching Skills for Leaders and Managers
    LinkedIn
    Sep, 2022
    - Nov, 2024
  • Coaching and Developing Employees
    LinkedIn
    Sep, 2022
    - Nov, 2024
  • Coaching for Results
    LinkedIn
    Sep, 2022
    - Nov, 2024
  • Communicating with Charisma
    LinkedIn
    Sep, 2022
    - Nov, 2024
  • Project Management Foundations
    LinkedIn
    Sep, 2022
    - Nov, 2024
  • Creating Your Personal Brand
    LinkedIn
    Sep, 2021
    - Nov, 2024
  • Effective Listening
    LinkedIn
    Sep, 2021
    - Nov, 2024
  • Managing Your Emotions at Work
    LinkedIn
    Sep, 2021
    - Nov, 2024
  • Organizing Your Remote Office for Maximum Productivity
    LinkedIn
    Sep, 2021
    - Nov, 2024
  • Remote Work Foundations
    LinkedIn
    Sep, 2021
    - Nov, 2024
  • Unconscious Bias
    LinkedIn
    Jul, 2021
    - Nov, 2024

Experience

    • United States
    • Business Consulting and Services
    • 300 - 400 Employee
    • Senior Principal Consultant
      • Aug 2021 - Present

      RQM+ is the leading MedTech service provider with the world’s largest global team of regulatory and quality experts. Building upon 40 years of regulatory expertise, we also provide comprehensive clinical trial, lab and reimbursement services – reducing risk and supporting market access throughout the entire product lifecycle for medical devices, digital therapeutics and diagnostics. With more former FDA, Medicines and Healthcare Products Regulatory Agency (MHRA) and notified body regulators than any other firm, the RQM+ team has deep expertise in all clinical specialties. RQM+ currently works for 19 of the top 20 medical device manufacturers and seven of the top 10 IVD companies. Show less

    • Switzerland
    • Medical Equipment Manufacturing
    • 700 & Above Employee
    • Senior Principal Quality Engineer, Vision Care R&D
      • Jul 2018 - Aug 2021

      Ensured new extended wear contact lens with proprietary coating was designed, developed, validated, and implemented with quality by design principles utilizing current Design Control and Risk Management practices. Ensured new extended wear contact lens with proprietary coating was designed, developed, validated, and implemented with quality by design principles utilizing current Design Control and Risk Management practices.

    • United States
    • Hospitals and Health Care
    • 400 - 500 Employee
    • Quality Technical Leader for New Product Development
      • 2014 - 2018

      Apply quality engineering principles in order to assure existing, new, or modified medical devices progressing through the product realization process deliver safe, effective devices that meet customer needs and regulatory requirements. Conduct internal and supplier audits as a Certified Quality Auditor. Apply quality engineering principles in order to assure existing, new, or modified medical devices progressing through the product realization process deliver safe, effective devices that meet customer needs and regulatory requirements. Conduct internal and supplier audits as a Certified Quality Auditor.

    • United States
    • Manufacturing
    • 700 & Above Employee
    • Quality Technical Leader
      • 2012 - 2014

      Apply quality engineering principles in order to assure existing, new, or modified products progressing through the product realization process deliver products which are safe, effective and meet customer and regulatory requirements. Conduct internal and supplier audits as a Certified Quality Auditor.

    • Senior Sterility Assurance Associate
      • 2006 - 2012

      Design and implement sterility assurance programs for new product development/commercialization of FDA Class I and Class II medical devices. Conduct supplier audits. Manage team's budget/project spending. Maintain compliance with regulatory agency requirements.

    • United States
    • Manufacturing
    • 700 & Above Employee
    • Clinical Education Manager
      • 2004 - 2005

      Key member of Scientific Affairs & Clinical Education team. Developed and delivered critical customer training programs to maintain existing business, generate new business and provide customers with continuing education units.

    • Research Scientist
      • 1998 - 2004

      Product development for FDA Class I medical devices. Led critical defense work against major competitors. Integrated products into the company post acquisition.

    • Sterilization Specialist
      • 1997 - 1998

      Designed & led sterilization validations, cycle optimization studies and product compatibility studies. Authored Standard Operating Procedures. Ensured compliance w/FDA/ISO/AAMI regulations. Represented company's sterilization activities in ISO, FDA & customer audits. Audited contract sterilization facilities & independent laboratories.

    • Sterilization Team Leader
      • 1996 - 1997

      Responsible for new facility start up. Designed & conducted product, process & equipment validations including external contract sterilizer validations. Co-authored & implemented quality system. Instrumental in receiving ISO certification. Trained other staff members.

    • Sterility Assurance Technician
      • 1994 - 1996

      Managed Sterilization Department & Microbiological laboratory. Conducted microbiological, chemical & environmental tests related to product sterility & release and process capability. Coordinated sterilization activities for all surgical products. Ensured compliance with FDA & ISO guidelines. Supervised 3 lab technicians. Represented corporation in ISO, FDA and customer audits.

    • Research Scientist
      • 1993 - 1994

      Developed ELISA based test kit for diagnosing von Willebrand's disease. Worked in Manufacturing department as needed for the production of various other ELISA tests. Conducted Quality Control testing to confirm product efficacy prior to distribution. Served as a company representative during FDA audits. Developed ELISA based test kit for diagnosing von Willebrand's disease. Worked in Manufacturing department as needed for the production of various other ELISA tests. Conducted Quality Control testing to confirm product efficacy prior to distribution. Served as a company representative during FDA audits.

    • United States
    • Higher Education
    • 700 & Above Employee
    • Research Assistant
      • 1988 - 1993

      Environmental sampling and study management of large scale epidemiological study on indoor air quality. Environmental sampling and study management of large scale epidemiological study on indoor air quality.

Education

  • University of Arizona
    B.A., Philosophy
    1987 - 1993
  • University of Arizona
    B.S., Molecular & Cellular Biology
    1987 - 1993

Community

You need to have a working account to view this content. Click here to join now