Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? 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 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.

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 be

- Develop procedures, work instructions and manuals of integral 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.).
- Preparation of technical presentations (PowerPoint, 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.

Who you are

- 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.
- You are meticulous and detail oriented.
- You have excellent communication and teamwork skills, as well as initiative and results orientation.

What we offer

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.





We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help.

Grifols is an equal opportunity employer.

Schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time).

Benefits package

Contract of Employment: Temporary position

Flexibility for U Program: Hybrid

Location: Sant Cugat del Vallès

more about Grifols

Type: Temporal tiempo completo

Job Category: AREA TECNICA OPERACIONAL

¿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.

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.

Mission

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.

What your responsibilities will be

- 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

Who you are

- 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.

What we offer

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.

We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help.

Grifols is an equal opportunity employer.

Flexibility for U Program: Occasionally Remote.

Benefits package

Contract of Employment: Permanent position.

Location: Sant Cugat del Vallès.

SPAIN : España : Sant Cugat del Valles : ((cust_building))

Type: Indefinido tiempo completo

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