¿Te gustaría unirte a un equipo internacional que trabaja para mejorar el futuro del sector de la salud? ¿Quieres contribuir a mejorar la vida de millones de personas? Grifols es una compañía global del sector de la salud que desde 1909 mejora la salud y el bienestar de las personas en todo el mundo. Somos líderes en medicamentos hemoderivados y medicina transfusional y desarrollamos, producimos y comercializamos medicamentos, soluciones y servicios innovadores en más de 110 países y regiones. ¿Quiénes somos

We believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities, fostering an inclusive environment where diversity makes us outstanding. Misión

To review and ensure that all procedures, testing methods and reports established in GEPD Plasma **Testing Laboratories** are in compliance to Egyptian regulations, and in accordance to cGMP, following Plasma Testing Specifications established and European Regulation. To manage and supervise Plasma Testing Laboratories Quality projects. To propose continuous improvement measures related to the quality systems of the Laboratories. To supervise the Quality Risk Management (QRM) process for the Laboratories. Responsabilidades

To review and ensure that all procedures established are in accordance to cGMP. To supervise GEPD Plasma Testing Laboratories quality system and quality culture. To ensure investigation for incidents are initiated, as well as root cause analysis are properly in place. To participate and support internal and external regulatory inspections and audits performed in the Laboratories. To manage and supervise Plasma Testing Laboratories Quality projects. Actively participate in Laboratory meetings for the follow-up of activities related to open Change Controls.



Coordinate the tasks required to be developed within the different areas of the company. Review new procedures and processes to be implemented in the Laboratory under the scope of the Change Controls open. To ensure continuous improvement measures related to the quality systems of the Laboratories. To supervise the monitoring of corrective and/or preventive actions implemented within the Laboratories. Ensure their proper implementation and effectiveness. To monitor quality system indicators. To propose improvements in the Laboratory's processes to enhance the quality system. To supervise the Quality Risk Management (QRM) process for the Laboratories. To supervise Quality Risk assessment studies and reports, as well as coordinate mitigation tasks. Candidato ideal

Bachelor's Degree in Life Sciences (Biology, Pharmacy, Biotechnology or related fields) Minimum 3-5 years of experience in a related field. Organized and able to manage time effectively. Ability to work within a highly regulated, labor intensive environment. Ability to understand, explain, follow, and enforce SOPs. Ability to plan, communicate and execute activities for the improvement of overall operations. Strong integrity and commitment to Quality and Compliance. Excellent oral and written communication skills to produce clear and concise factual findings. Advanced level of Spanish and English. This position requires significant travel and on-site presence in Egypt, with approximately 50% of the role based in Egypt. Incentivos

It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment. Grifols is an equal opportunity employer. Contrato y ubicación

Contract: Permanent position. Location: Sant Cugat del Vallès, Spain.

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📌 Pharma Qa & Compliance Officer — Barcelona (Temp)
🏢 Actual Group
📍 Barcelona