Nuria Alegre Email & Phone Number

Rafelbunyol, Vc, Es

Valencia Y Alrededores, España

Pharmacist responsible in charge of training Pharmacy staff in Valencia and Castellon in Boehringer products.

Manage customer experience reports (complaints) in compliance with applicable regulations.Manage SAE clinical trials from database Medidata ,e-medidata and Oracle.Receive, initiate, document, coordinate the investigation and close the complaint files accordinglyDetermine the reportability to the authorities according to the internal procedures and ISO 13485Prepare and submit Vigilance report to the Authorities. Link CAPA’s to the investigation as part of the file.Perform the trends for the failure and include them in the file.Inform the customer when required.Provide technical support for external and internal customer inquiries.

Give support to the sales team regarding all related to Grant procedures and organising Events,Congresses,Wetlabs,Sales meetings...

Implement CAPA project

*Deal with Regulatory Affairs topics in Spain and PortugalCheck label /packaging compliance, communication compliance activities, updating on Spanish and Portuguese regulations related to product compliance, support in case of QA and RA related incidents/issues, under the Europe Regulatory Manager supervision. Coach Marketing, local translators and agencies to make correct translation first time.Check, comment and approve :-marketing communication (advertising, leaflets, web sites etc).- promotional items.Support recall processes (Portuguese and Spanish Market)Maintain updating on specific Spanish and Portuguese Regulations about products complianceJDE release products.** Deal with risk prevention activities: -mantain and update risk prevention plans and procedures-Health vigilance ,EPI'S, trainings,fire drill ,external coordination activities, control of radiation exposure measures,luxes,dB,ergonomics,in itinere accidents...

Pharmacist responsible in charge of trainining Pharmacy staff of Valencia and Castellón in Glaxo products.

Quality Engineer handling AUDI and environmental processes ,ISO14000, ISO TS16949Monitor, test and inspect products to assure that they meet specified standards.Provide customer quality improvement information by identifying testing methods and samples relevant to manufacturing processes. Develop sampling plans .Maintain quality process controls. Prepare test reports and make material recommendations. Maintain professional and technical knowledge. Contribute to team effort by accomplishing related results as needed. Update and mantain environmental procedures and coordinate internal audits.Control of waste treatments.

Regulatory affairs manager of Veterinary Warehouse Laboratory Quality Manager (Microbiological, Physical–Chemical studies in Raw materials and Foodstuffs) Quality and Occupational Risk Prevention management.OSHAS18001 Stablishment of ISO 9000 Standard, HACCP.Legal compliance documents and procedures with Conselleria de Sanidad.Control of veterinary drugs of the bussines pharmacy.Drug dispensations,stock and temperature control,management plans,interaccions.Microbiological, Physical–Chemical studies in Raw materials and Foodstuffs. ,Develop and set up of Quality and Risk prevention management plans, emergency plans, machinery and technical instructions for analysis, supplier control ,non conformances and corrective actions, internal and external audits.

Carné De Usuario Profesional De Productos Fitosanitarios Nivel Cualificado

60 horas totales de curso

Master En Prevencion De Riesgos Laborales, Salud Laboral Y Prevención De Riesgos Laborales

Especialidades: Ergonomia y psicosociología Higiene ambiental Seguridad en el trabajo

Master En Calidad Ambiental

Calidad y Medioambiente

Farmaceutica

Farmaceutica

Education record