Maria Lucrecia A
About
Maria Lucrecia A is from Argentina. Maria Lucrecia works in the following industries: "Pharmaceuticals". Maria Lucrecia is currently Director técnico at Hisan S.A , located in Gran Buenos Aires, Argentina. In Maria Lucrecia's previous role as a Quality Assurence Logistics & Distribution, Senior Coordinator at GSK, Maria Lucrecia worked in Argentina until Sep 2017. Prior to joining GSK, Maria Lucrecia was a Quality Assurance Analyst at Novartis and held the position of Quality Assurance Analyst at Argentina. Prior to that, Maria Lucrecia was a Pharmacist in Community Pharmacy at Farmacia oficinal, based in Argentina from Aug 2011 to Aug 2012. Maria Lucrecia started working as Analyst of Galenic Develop at Laboratorio Elea in Argentina in Sep 2010. From Apr 2009 to Aug 2010, Maria Lucrecia was Qualified Professional at Laboratorios Mar, based in Argentina.
You can find Maria Lucrecia A's email address at finalscout.com. FinalScout is a free professional database with over five hundred million business professional profiles and over two hundred million company profiles.
Maria Lucrecia A's current jobs
Part time
Maria Lucrecia A's past jobs
Performed investigations related to deviation during transport of medical devices, effectiveness check of Corrective actions and preventive actions (CAPAs) and change controls associated with assigned Logistics Service providers, warehousing and distribution facilities are properly performed. Establish Quality Assurance Agreement with Logistics Service providers, warehouses and distribution facilities. Assist the audit team in national and international audit preparation and participate in the execution of assigned warehousing and distribution facilities. Provide assistance to implement the Distribution Risk Assessment (DRA). Recall execution and annual mock. Risk assessment. Auto-inspections and audit in Logistics Service providers. Perform surveillance on new/upcoming regulations related to Distribution and Logistics. Create & review Key Performance Indicators (KPI).
Create and review Standar Operations Procedures (SOPs) and training them. Review and follow up customer complaints, deviations, change control and effectiveness check of corrective action and preventive actions (CAPAs). Reviewed and performed master batch records. Provide assistance to Product Release activities. Provide assistance to support Regulatory submissions. Provide assistance to support Product Transfer. Control the status of Annual Product Review (APR/PQR). Provide assistance to establish Quality Agreements with 3rd Parties. Provide assistance to coordinate the Recall process. Create & review Key Performance Indicators (KPI). Follow up validations process. Novartis is an international Pharmaceutical Industry of drugs.
Recepción y elaboración de pedidos, dispensación de medicamentos, control de stocks, caducidades y obras sociales, devoluciones de medicamentos, gestión de recetas, organización de horarios, asentamiento de estupefacientes y psicotrópicos en libro recetario, emisión de pagos, desarrollo galénico.
Design and write Pharmaceutical Development Monographs for the Common Technical Document (CTD). Write production guidelines, develop and manufacturing of pilot batches, Research and develop of preformulation Studies and pharmaceutics, follow up of the manufacturing process in industrial scale and process transfer to third party under current Good Manufacturing Process (cGMP’s).
Quality Assurance