Quality Technician

Grifols; Sant Cugat del Vallès; Híbrido; EUR 42.000 - 60.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Hybrid work arrangement

Descripción de la vacante

Grifols is seeking a Quality Specialist to join the Good Distribution Practice (GDP) Compliance team in an international setting. You will support the Technical Management personnel of the company's subsidiaries and partners, ensuring quality standards are met across contracts, serialization, and documentation systems.

The ideal candidate holds a Life Sciences degree with pharma/medical devices experience, strong English, and proficiency in SAP and Microsoft Office.

Formación

• Bachelor's degree in Life Sciences (Pharmacy, Chemistry or similar). Master's preferred.
• Experience in pharma or medical devices; good knowledge of GxP.
• Advanced English and strong MS Office skills.
• Knowledge of SAP is valued.

Responsabilidades

• 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.
• Request, coordinate, review and compile information requested by Headquarters.
• Prepare technical presentations (PowerPoint, etc.).
• Provide technical support to subsidiaries in documentation systems and Quality System tools.
• Support training processes for SOPs.

Conocimientos

English - Advanced

Attention to detail

Communication & teamwork

Initiative & results oriented

Educación

Bachelor's degree in Life Sciences

Master's degree in Pharmaceutical Industry or related area

Herramientas

SAP

Microsoft Office

Descripción del empleo

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 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.).
• 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

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions).

• 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.

Information about Grifols is available at www.grifols.com.

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, 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).

Contract of Employment:

Temporary position

Flexibility for U Program:

Hybrid

Location:

Sant Cugat del Vallès

www.grifols.com

Learn more about Grifols