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CQC Manager Testing Quality Review. Arr. Nivelles. Bélgica

Contratación de Ingenieros electrónicos en Bélgica (Arr. Nivelles)



Clasificación del trabajo: Profesionales científicos e intelectuales : Profesionales de las ciencias y de la ingeniería : Ingenieros no clasificados bajo otros epígrafes : Ingenieros electrónicos.
Intellectuele, wetenschappelijke en artistieke beroepen : Wetenschappers en ingenieurs : Ingenieurs op het gebied van de elektrotechniek, elektronica en telecommunicatie : Elektronica-ingenieurs.

Descripción de la oferta de trabajo:

Basic qualifications: - Ph.D. in Analytical Chemistry, Biochemistry, or related field - Ideally Green Belt certified - At least 5 years of experience in pharmaceutical industry is an asset - Experience in biochemical, biological and/or physico-chemical assay

Preferred qualifications: - Good Knowledge in cGMP - Experience in project management and change management - Demonstrated ability to work in multi-disciplinary teams, displaying excellent interpersonal, organizational, and communication skill - Good communication skills towards internal clients (commercial teams, product coordinators, QA, RA, ...) - Autonomous and proactive - Scientific and documentary rigor - Lab-oriented - Able to manage several project simultaneously - Able to interact with several internal clients simultaneously - English written & spoken - Goof Knowledge of Microsoft Office (mainly Excel and MS project)

 

Details: Job Purpose: In the team Analytical method Remediation, the manager has the accountability of the Testing Quality Review process. This process allows identification of methods at risk for the business and ensures that action plan is defined and execute according to CQC priorities. Key Responsibilities: - Lead the Testing quality review process: - accountable for the scoring of CQC methods, - accountable and responsible of report generation   - Accountable that the CQC has an approved remediation plan for methods at risk. - Accountable for the in use status of the project by tracking process progress, following specific KPI and reporting to the defined governance. - Coordinate and facilitate the initial evaluation of high and medium risk methods. - Coordinate and lead investigation of significant analytical and quality issues in order to guarantee the continuity of supply and in accordance with the current regulations - Continuous improvement of this new process and tools used for the scoring Our Department: Global Quality Departments is responsible for setting up all global rules and regulations to ensure GSK vaccine products are manufactured, tested, released and distributed in compliance with regulatory requirements. The QA Belgium departments manage all product quality related activities in industrial operations in Belgium, including regulatory compliance. The scope covers any action that potentially impacts final product quality. The QA Belgium department is also responsible for the release of final products made in Belgium and abroad. Quality for Research & Development in partnership with R&D teams promotes quality and enables them ensuring activities of Research & Development are delivered in a compliant and sustainable way, in order to guarantee patient safety, company and regulators satisfaction, as well as successful product pipeline delivery.

Zie Functieomschrijving

Zie Functieomschrijving

Servicio de empleo de origen: VDAB, Servicios Públicos de Empleo, Bélgica.

País del trabajo: Bélgica.

Región: Arr. Nivelles.

Ver 34 ofertas de trabajo en "Arr. Nivelles" (Bélgica).

Fecha de inicio: 22/06/2017.

Nº de vacantes: 1.

Experiencia: Más de 5 años.

Tipo de contrato: Jornada completa.

Duración del contrato: Indefinido.

Cómo solicitar: Otros (véase la descripción).

Cómo solicitar el puesto:

Empresa: Vacature.com.

Dirección: Vacature.com, Havenlaan 86C bus 101, 1000 BRUSSEL, BELGIE.

Contacto: notApplicable





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