Quality Control Lead - Pharmaceuticals. en Michael Page

Quality Control Lead - Pharmaceuticals.
Michael Page | (21) ofertas activas
Madrid 12 Feb.
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Descripción

We are looking for a Quality Control Lead to manage the analytical and support activity of the laboratory, supervising the analysis of materials and products in compliance with approved working procedures.

Detalles del cliente

Pharmaceutical Company

Descripción de la oferta


  • Approves analyses of raw materials, packaging materials, intermediate products, finished products and stabilities.

  • Guarantees the operation of the laboratory, including its economic and training aspects, ensuring that the staff of the department receives initial and continuous training adequate to the needs.

  • Organises, performs and ensures the analysis activity to obtain the conformity opinion of the batch, within the established time of the production programme.

  • Supervises the management of the correct investigation of out-of-specification and/or trend analyses.

  • Drafts and/or approves specifications, sampling instructions, methods of analysis, and other Quality Control procedures, ensuring that they are respected and ensuring continuous revision.

  • Ensures the maintenance of the sampling library, standards, equipment and analytical records.

  • Ensures compliance with the Stability Programmes established for the products.

  • Proposes any improvement in analytical techniques, ensuring that the necessary validations are carried out.

  • Participation in external and internal audits.

  • Ensures that the Quality processes in the laboratory are implemented and maintained.

  • Promotes and participates in continuous improvement processes in the Quality Control laboratory.


Perfil del candidato


  • Degree in Pharmacy or similar, with proven experience in the Pharmaceutical Industry in the area of Quality Control.

  • Knowledge of Good Manufacturing Practice (GMPs), Regulation (EU) 2017/745 of the European Parliament and of the Council on Medical Devices and FDA 21 CFR".

Oferta de empleo

Oportunidades de carrera y desarrollo profesional.


Número de vacantes: 1
Modalidad de trabajo: Presencial
Tipo de contrato: Full-Time
Remuneración anual: Negotiable
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Requisitos
Degree in Pharmacy or similar, with proven experience in the Pharmaceutical Industry in the area of Quality Control.
Knowledge of Good Manufacturing Practice (GMPs), Regulation (EU) 2017/745 of the Eu

Estudios mínimos
Diplomado
Experiencia mínima
de 5 a 10 años
Disponibilidad para viajar
El 20% del tiempo laboral

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