Antonio Enes

I Have worked in the Pharmeceutical industry for over 9 years. • Ensure QA coverage supports production schedule • Train new QA Specialists • Review and approve all executed batch records ensuring compliance with cGMPs and all applicable SOPs. • Responsible for inspection of manufacturing/filling lines by performing line checks and line clearances. • Responsible for initiating change controls for SOP’s, MBR’s and other documentation. Ensure document change order process is efficient and compliant. • Responsible for retention samples and archiving. • Responsible for inspecting and approving raw materials used in production. • Responsible for validation protocols and summary reports. • Periodically perform audits on suppliers and/or contract manufacturers. • Initiate deviations, corrective and preventative actions and change orders when necessary. Assist with determining root cause, product impact and corrective and preventative actions. Previously i worked in the Banking Industry as a Senior Operations Clerk. My areas of focus included: * Responsible for leading a team of 4 in achieving all duties and responsibilities. * Responsible for achieving certain goals. * Responsible for communicating and implementing changes to policies and procedures. * Ensured that team exceeds customer satisfaction. * Motivated staff to maximize their resolution goals. * Acted as Department supervisor in absence of Management. * Motivated team in focusing on tasks assigned.