Wallace Yopp

Validation Consultant at ProPharma Group
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Contact Information
us****@****om
(386) 825-5501
Location
US

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5.0

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Tom Wittliff

Working for Wallace in his roll as manager was an extremely positive experience due to his motivation, dedication and knowledge. There are few people that I have met that are as hard working as Wallace and he is very result oriented.

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Credentials

  • Project Management: Preventing Scope Creep
    LinkedIn
    Sep, 2018
    - Nov, 2024
  • Body Language for Leaders
    LinkedIn
    Jun, 2018
    - Nov, 2024

Experience

    • United States
    • Business Consulting and Services
    • 700 & Above Employee
    • Validation Consultant
      • Aug 2022 - Present

    • United States
    • Chemical Manufacturing
    • 1 - 100 Employee
    • Vice President of Manufacturing & Quality Control
      • Oct 2020 - Aug 2022

      Responsible for starting up new facility and resuming commercial production activities following a facility transfer from Flagstaff to Phoenix. Responsible for starting up new facility and resuming commercial production activities following a facility transfer from Flagstaff to Phoenix.

    • United States
    • Business Consulting and Services
    • 700 & Above Employee
    • Validation Consultant
      • Jan 2019 - Dec 2019

      Lead Validation Consultant/ Project Manager for new Prefilled Syringe Line Lead Validation Consultant/ Project Manager for new Prefilled Syringe Line

  • Celgene
    • Phoenix, AZ
    • Director of Manufacturing
      • Oct 2014 - Aug 2017

      * Department head for manufacturing operations. * Working closely with all support groups to prepare MFG for increaseing our production capacity. * Applying situational leadership for management and staff development. * Department head for manufacturing operations. * Working closely with all support groups to prepare MFG for increaseing our production capacity. * Applying situational leadership for management and staff development.

    • Director, Validation and Technical Services
      • Oct 2008 - Oct 2014

      * Established a high performing Validation and Technical Services group and validation programs for new facility start-up, qualification and commercial manufacturing. * Prepared site for PAI and regulatory approval. * Responsible for site Project Management and site Technical Training functions * Established a high performing Validation and Technical Services group and validation programs for new facility start-up, qualification and commercial manufacturing. * Prepared site for PAI and regulatory approval. * Responsible for site Project Management and site Technical Training functions

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Director, Validation & Technical Services
      • Oct 2008 - Aug 2014

      Obtained regulatory approval for US,EU, PMDA and working on various ROW market(s). Responsible for site validation, technical services, metrology and project management. Shifting from facility start-up to routine commercial manufacturing. This includes CI initiatives, day to day support and strategic risk mitigation projects. Obtained regulatory approval for US,EU, PMDA and working on various ROW market(s). Responsible for site validation, technical services, metrology and project management. Shifting from facility start-up to routine commercial manufacturing. This includes CI initiatives, day to day support and strategic risk mitigation projects.

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Validation Manager
      • 1993 - 2008

    • Validation Manager
      • 1993 - 2008

Education

  • Campbell University
    1998 - 2001

Community

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