Quality Specialist - Good Distribution Practice (GDP) Compliance
Would you like to join an international team working to improve the future of healthcare? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
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.
Develop procedures, work instructions and manuals of global 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.
Bachelor's Degree in Life Sciences field (Pharmacy, Chemistry or similar). 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 16-19h and Friday 8-15h (with the same versátil start time).
Contract of Employment: Temporary position
Hybrid
Contract Logistics Quality Specialist Healthcare
Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. From 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.
You 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 Model
Monday-Thursday 7-10 to 16-19h and Friday 8-15h. (Contract of Employment: Permanent position
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 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.
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.
To supervise GEPD Plasma Testing Laboratories quality system and quality culture.
To ensure investigati

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