Experience

• 

  Abbott

  Nov 2001 - Jul 2002

  Production operator

  Responsible for inspecting and packaging plastic parts

• 

  Allergan

  Aug 2002 - Feb 2010

  HR Training - Responsible for data entry of training records into data base. Helped with the development and implementation of the Learning Management System. Managed the 5S program for the site. Developed, maintained and published training metrics.Non-Inventory Purchasing - Responsible for the conversion of paper requisitions to Purchase orders in SAP. Developed a comprehensive non-inventory purchasing program for the site. Became the SME for Non-inventory purchasing for the site for auditing agencies. Helped develop and implement an electronic purchasing system for the company. Helped redefine the Spare Parts purchasing process. Became the SME for the Spare Parts purchasing process representing the site in audits. Show less

  • Sr. HR Coordinator

    Sept 2005 - Feb 2010

  • Plastics Production Coordinator

    May 2004 - Sept 2005

  • Sr. Plastics Process Technician

    Aug 2002 - May 2004
• 

  Allergan

  Oct 2010 - now

  Coordinate and manage all training for the site, including administering the Learning Management System. Collaborate and develop training, programs, and modules for all levels of employees at the facility. Create e-learning modules for training in the Learning management System. Develop and publish training metrics. Interface with auditing agencies for training. Continuously develop new projects to raise the training standard for the site. Manage the Qualified Trainer Program. Deliver and maintain cGMP related training. Ensure compliance with regulatory criteria including the FDA, European Community (EC), ISO 13485:2003- Medical Devices, European Economic Community Medical Device Directive (MDD), Canadian Medical Device Regulations (CMDR), Canadian Medical Devices Conformity Assessment System (CMDCAS), OSHA, Sarbanes-Oxley, EPA, EEOC, and ADA. Show less Coordinate and manage all training for the site including administering the Learning Management System. Collaborate and develop training, programs, and modules for all levels of employees at the facility. Create e-learning modules for training in the Learning management System. Develop and publish training metrics. Interface with auditing agencies for training. Continuously develop new projects to raise the training standard for the site. Manage the Qualified Trainer Program. Deliver and maintain cGMP related training. Ensure compliance with regulatory criteria including the FDA, European Community (EC), ISO 13485:2003- Medical Devices, European Economic Community Medical Device Directive (MDD), Canadian Medical Device Regulations (CMDR), Canadian Medical Devices Conformity Assessment System (CMDCAS), OSHA, Sarbanes-Oxley, EPA, EEOC, and ADA. Show less

  • Quality Training Manager

    Mar 2016 - now

  • Sr. cGMP Trainer

    Feb 2015 - Mar 2016

  • cGMP Trainer

    Feb 2013 - Feb 2015

  • Associate Systems Support Admin

    Oct 2010 - Feb 2013