Global Quality Specialist — Pharma, GDP/GxP

Grifols, S.A; Sant Cugat del Vallès; On-site; EUR 45,000 - 60,000; Full time

Job summary

Grifols SA seeks a Quality Specialist to join the GDP Compliance department. The role supports Technical Management across subsidiaries and partners in an international setting, focusing on global quality processes and regulatory alignment.

Responsibilities include developing SOPs, managing quality data, coordinating contracts, and delivering training in quality systems. The ideal candidate has pharma experience, strong English, and meticulous attention to detail.

Qualifications

• Bachelor's Degree in Life Sciences; Master's in Pharmaceutical Industry or related area is a plus.
• Valuable experience in a similar role within pharma industry and/or medical devices.
• 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.
• Meticulous and detail oriented.
• Excellent communication and teamwork skills, as well as initiative and results orientation.

Responsibilities

• 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 contracts are signed and reviewed by the relevant department and fees paid where appropriate.
• Request, coordinate, review and compile global information that Headquarters requests from subsidiaries.
• 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.

Skills

Advanced English

Microsoft Office

SAP knowledge

Attention to detail

Education

Bachelor's Degree in Life Sciences

Tools

SAP

Job description

Grifols SA seeks a Quality Specialist to join the GDP Compliance department. The role supports Technical Management across subsidiaries and partners in an international setting, focusing on global quality processes and regulatory alignment.

Responsibilities include developing SOPs, managing quality data, coordinating contracts, and delivering training in quality systems. The ideal candidate has pharma experience, strong English, and meticulous attention to detail.