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Experience

    • Canada
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Vice President of Operations
      • Oct 2021 - Present

    • Director Of Engineering
      • Sep 2019 - Sep 2021

    • Regulatory Policy and Risk Management Advisor
      • Apr 2020 - May 2020

      Installation, commissioning and qualification of two TSI 8130A Filter Testers. Training and coaching of testing staff on the operation and the testing of respirators and other filtration media. Writing of internal Operation and Preventive Maintenance procedures

    • United States
    • Pharmaceutical Manufacturing
    • 500 - 600 Employee
    • Medical Device Development Engineer
      • Feb 2018 - Sep 2019

    • Systems Engineer
      • Jul 2015 - Feb 2018

    • Engineering Supervisor
      • Oct 2012 - Jul 2015
      • Montreal, Canada Area

    • Canada
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Lyophilization Engineer
      • Dec 2010 - Oct 2012

      Support a Lyophilized injectables production line and auxiliary systems:- Recommend and coordinate continuous improvement efforts.- Coordinate preventive and corrective maintenance activities.

    • Validation Engineer
      • Mar 2010 - Dec 2010

    • Project Engineer
      • Nov 2009 - Feb 2010

      -Develop and write User Requirement Specifications for OSD manufacturing equipment-Source and purchase manufacturing equipment according to URS-Aid in Commissioning activities-Work with Production, Continuous Improvement, Quality, and Health & Safety representatives to develop manufacturing room layouts-Support Validation and Technical Writing departments in their activities related to new equipment

    • President
      • Sep 2002 - Dec 2009

      - Manage validation projects for over 10 clients in the Montreal area- Validation of Steam-In-Place (SIP) Sterilization Systems.- Validation of Autoclaves (microbiology and production).- Validation of Incubators and Freezers.- Validation of USP Purified Water Systems.- Validation of Water-for-Injection System and Pure Steam Generators.- Validation of Compressed Air Systems.- Validation of Pharmaceutical Packaging Equipment.

    • Engineering and Plant Manager
      • Dec 2005 - Jun 2009

      - Supervise Engineering and Maintenance department.- Manage equipment and prototype design, installation and validation projects.- Manage the cGMP upgrade project for the production area- Participate in product-launch teams.- Supervise testing within engineering laboratory.- Supervise production of Triosyn resin.- Develop R&D test plans for raw media and finished products.- Implement cGMP and ISO 13485 practices and procedures within the engineering department.- Develop and manage Preventive Maintenance and Calibration programs.

    • Consultant in Validation
      • Sep 2003 - Sep 2005

    • Consultant - Validation
      • 2002 - 2005

    • Validation Coordinator
      • Jan 2002 - Mar 2003

    • Validation Specialist
      • Jan 2000 - Dec 2001

    • Validation Specialist
      • May 1999 - Dec 1999

Education

  • 1995 - 1999
    Concordia University
    Bachelor in Mechanical Engineering
  • 2011 - 2011
    McGill University
    Certificate, Lean Project Leader
  • Laurier Macdonald

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Industry Focus. “Pharmaceutical Manufacturing”

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