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No se requiere experiencia
Retribución sin especificar
Calidad, I+D, PRL y medio ambiente
Técnico
1
0
Contrato Indefinido
Jornada Completa
Duración de la oferta: hasta el 07/06/2022.
* Responsible for ensuring the GMP- and regulatory conform production of medicinal drugs acc. to guidelines e.g. EU-GMP-Guideline… * Review the technical content of SOPs for manufacturing and Quality Control. * Supports the GMP conform process optimization in manufacturing and Quality Control. * Quality review of batch documentation for release purposes * Maintaining of the OOS-/ Deviation system in the company * Maintaining of the Complaint system in the company * Compiles the Deviation Reports together with other Departments * Pharmaceutical assessment of deviations and ensuring of appropriate CAPAs * CAPA-management together with other departments * Maintain SOP´s updated, create new ones if needed and propose improvements to existing ones. * Maintain the Qualification / Calibrations System updated, coordinating tasks with other departments. * Coordinates and accompanies validation activities in manufacturing and Quality Control * Preparation of Validation Protocols in-time * Co-operation and participation in audits and subsequent measures * Coordinate the necessary IT validations * Release of batches according GMP rules
* Degree in pharmacy * Experience under GMP environment * Minimum two years of experience as a Quality Assurance Technician * High level of English
* Indefinite-term contract from the beginning * Excellent working environment * Competitive salary
Important animal health pharmaceutical laboratory is looking for a QA Technician & QP Deputy
Al pulsar el botón “Inscribirme a la oferta”, Usted consiente que Infoempleo, S.L. comunique sus datos de carácter personal para participar en futuros procesos de selección a los ficheros de Page Personnel con domicilio social en Paseo de la Castellana, 28 3ª planta 28046 MADRID, Madrid donde podrá ejercitar sus derechos de acceso, rectificación, cancelación y oposición.
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