Amanda Ridgeway

Background

About Amanda Ridgeway

Over fifteen years of experience, in the active pharmaceutical ingredient industry. Excelling as a US and ROW Regulatory Affairs professional, a Sr. Analytical Scientist, and a Program Supervisor. Currently as a Project Manager in Regulatory Affairs, I work with new product introduction teams to ensure development and validation activities provide all necessary documents I require for writing, publishing, and submitting a US DMF, CEP, and/or ROW filing. During my tenure as an Analytical Scientist, my ability to interpret complex data and identify trends has been integral to the flawless execution of analytical validations and the timely resolution to plant investigations. My effective communication skills have allowed me to routinely present technical data in a manner that acquires approval and support from non-technical audiences. The revitalization of the Reference Standards Program to improve quality and compliance was driven by my technical knowledge and my in depth understanding of customer needs. Due to excellent customer service, effective advertising of our current portfolio, and continual addition of new reference standard products the external sales grew substantially. In summary, my analytical and logical nature and my nurturing customer focus along with my adept leadership and communication skills will be irreplaceable assets.