Quality Specialist - Good Distribution Practice (GDP) Compliance¿Interesado en saber más sobre este trabajo? Desplácese hacia abajo y descubra qué habilidades, experiencia y cualificaciones académicas se necesitan.Grifols is a global healthcare company that since has been working to improve the health and well-being of people around the world. We are looking for a Quality Specialist to join Good Distribution Practice (GDP) Compliance department at Grifols SA.This person will support the team and the Technical Management personnel of the company's commercial subsidiaries and/or internal or external partners in an international environment.What your responsibilities will beDevelop procedures, work instructions and manuals of general international scope.Track affiliate quality KPIs and prepare reports, collect, review and compile data in Excel.Coordinate and update contracts, rates and local medicine serialization requirements, ensuring that necessary contracts are signed and reviewed by the relevant department and that fees are paid where appropriate.Request, coordinate, review and compile global information that Headquarters requests from subsidiaries (corporate responsibility report, Retention Polices, etc.).

Provide technical support to subsidiaries in documentation systems and use of Quality System computer tools.Provide support in the process of training in SOPs.Master's degree in Pharmaceutical Industry or a related area is a plus.Valuable experience in a similar role within pharma industry and/or medical devices.Valuable to have knowledge of regulations in the Quality field, such as GxP.Advanced level of English.Proficient user of Microsoft Office.Knowledge of SAP is a valuable.Schedule: Monday-Thursday 7-10 to h and Friday 8-15h (with the same flexible start time).

Temporary positionFlexibility for U Program: HybridLocation:



Sant Cugat del VallèsContract Logistics Quality Specialist HealthcareWould you like to join an international team working to improve the future of healthcare? Grifols is a global healthcare company that since has been working to improve the health and well-being of people around the world. MissionFrom Quality Assurance we are looking for a Corporate Quality Auditor who will be the responsible to perform the Corporate Quality audits to the companies of Grifols Industrial group and affiliates, in order to evaluate and ensure the compliance of Good Distribution Practices, internal procedures and internal policies as well as to detect opportunities for improvement and best practices.

Audits will be performed to Biopharma, Diagnostic and Healthcare busines units manufacturing sites (Pharmaceutical products and Medical Devices) and Grifols Affiliates.Conduct Corporate Quality Audits, ensuring compliance with the approved audit plan, scope, and timelines.Evaluate, classify, and document audit findings according to established quality standards, providing practical recommendations for improvement.Follow up on corrective and preventive actions (CAPAs) derived from audits, monitoring implementation and effectiveness.Support the management, monitoring, and reporting of quality indicators and key performance metrics within the area.Ensure adherence to corporate quality standards, regulatory requirements, and internal procedures throughout the audit process.Who you areYou have a Life Sciences Degree (Pharmacy, Biology, Chemistry, Biotechnology) or Engineering Degree (Chemical or Industrial) or 10 years experience.Advanced English level, both written and spoken.Hybrid ModelFlexible schedule: Monday-Thursday 7-10 to h and Friday 8-15h. (Permanent positionLocation: Quality Specialist - Good Distribution Practice (GDP)



Compliance (Spanish)¿Te gustaría unirte a un equipo internacional que trabaja para mejorar el futuro del sector de la salud? ¿Grifols es una compañía global del sector de la salud que desde **** 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.MissionTo 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.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 manage and supervise Plasma Testing Laboratories Quality projects.Actively participate in Laboratory meetings for the follow-up of activities related to open Change Controls.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. 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.Strong integrity and commitment to Quality and Compliance.Advanced level of Spanish and English.Occasionally Remote.Permanent position.

📌 Shift Quality Control Technician (Barcelona)
🏢 Greif
📍 Barcelona