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Al menos 3 años de experiencia
Retribución sin especificar
Calidad, I+D, PRL y medio ambiente
Técnico
1
3
Contrato De duración determinada
Jornada Completa
Duración de la oferta: hasta el 23/08/2018.
- Assuring compliance with established policies/procedures of MMD and Corporation and complies with all applicable governmental regulations (GMP, etc.) - Acting in conjunction with the External Site Quality . - Responsible for coordination, oversight, and communication on matters related to the GMP status of the external manufacturer. - Tracing and monitoring operational and quality performance of the external party/partner. - Performs change control assessments and approvals. - Review and approves master batch records. - Providing on-site guidance in the preparation of metrics, procedures, and guidelines where warranted. - Provides guidance to the external partner on conducting investigations, customer complaints, etc. where warranted. - Prepares Annual Product Quality Review.
- Experience with biologics Quality Assurance, SAP based MRP platform and Trackwise change control - English written and spoken. - Possesses a combination of analytical/scientific skills in order to effectively manage and control all activities necessary to support a total Quality Operations program governing external parties/partners that manufacture, package, analyze, release, store and/or distribute Therapeutic Protein and Biological products.
Salario mínimo:28000 bruto/anual Jornada completa. Obra y servicio. Ubicación: Madrid
Importante empresa del sector farmacéutico.
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