QUALITY CONTROL MANAGER ONCOLOGY - ALGERIA

International Permanente EUR95.225 - EUR114.271 por año Ver descripción del puesto
Based in Algiers, you will be responsible for managing, reviewing and overseeing relevant quality control (chemicals & microbiological) activities and practices related to the job function by ensuring integrity and traceability of all generated data in accordance with the current SOPs and contributing to the development and implementation of quality standards /& principles.

Actualizado el 27/07/2026

  • Leading Pharma group
  • Experience in injectables, vaccines or Oncology products mandatory

¿Dónde vas a trabajar?

Our client is a leading pharma group

Descripción

You will be responsible of the following tasks:

-Supervise the implementation of the Quality Control function plans, and ensure their compliance with client quality system

-Develop the quality control function's work plan; assign work activities, projects and programs, review and evaluate analytical methods and procedures, and directing the quality control activities to serve the QC department objectives.

-Ensure that qualification/validation and maintenance of the QC Laboratory premises and equipment/instruments are appropriately performed

-Develop and maintain quality control procedures by ensuring completion of all tests, studies, reports and investigations in an accurate, effective and timely manner

-Review and evaluate all data generated according to written procedures and recommend on the release or reject of the analyzed items (raw materials, packaging materials, intermediate, bulk and finished products)

-Contribute for evaluation and qualification of vendors of raw materials and packaging materials.

-Inform all involved functions of any rejects and non-conforming results related to raw materials, packaging materials, finished products, and any other area monitored by QC testing

-Lead the execution of investigations on relevant QC issues (OOS/OOT/deviations),verification results and determine corrective and preventive actions as per defined SOPs

-Develop and validate the analytical methods in accordance with the current regulations and apply the latest technical methods

-Validate the analytical test procedures, specification sheets, SOPs (pharmacopoeia and In-house). Review and approve documents related to QC function activities (procedures, protocols, reports, etc.)

-Establish and maintain a tracking and trending system of QC issues (OOS /OOT)

-Conduct performance appraisals for subordinates according to scheduled plans and recommend necessary actions as per the applied practices

-Co-ordinate technical audits of the QC Laboratory to determine the analytical quality systems are yielding the highest quality information and to ensure that the analytical instrumentation is functioning properly and calibration and servicing is as per schedule.

¿A quién buscamos (H/M/D)?

Pharmacist, Engineer /Master (Chemistry /Biology).

(10) years (or more) in a similar position within pharmaceutical company.

¿Cuáles son tus beneficios?

Attractive package

Ver más ofertas de empleo
Mehdi Boutaleb
Indicar número de referencia para la oferta
JN-022025-6671749

Resumen de empleo

Sector
Ingenieros
Sub Sector
Salud, Seguridad y Medio Ambiente
Añadir industria
Healthcare / Pharmaceutical
Localización
International
Tipo de Contracto
Permanente
Nombre del consultor
Mehdi Boutaleb
Número de referencia
JN-022025-6671749

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