Quality Technician

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

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.

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

SAP / Grifols

SAP as service provider:

Grifols: