Quality Contracts Manager

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.

Help us lead one of the world’s largest pharmaceutical companies. We are a world leader in plasma-derived medicines with a presence in more than 100 countries, and a growing global team of over 20.000 people. That’s why we need a Quality Contracts Manager like you to join at Grifols SA.

Your mission will be to ensure that responsibilities related to GxP activities are clearly defined, documented and fulfilled across the international network of donation centers, fractionation plants, quality control laboratories, logistics areas, and strategic partners, in accordance with global regulatory requirements and Grifols’ corporate Quality policies.

• Coordination of the Group’s Quality Agreements:

Lead the drafting, review, negotiation and approval of Quality Agreements with the different Group divisions and with external partners at a global level (suppliers, laboratories, contract manufacturers, distributors, etc.).

Ensure that Quality Agreements are aligned with international regulatory requirements (FDA, EMA, Health Canada, MHRA, PMDA, among others) and with corporate policies and standards (EU GMP, 21 CFR, ICH Q10, ISO 9001, PPTA).

Collaborate cross-functionally with Legal, Procurement, Regulatory Affairs, Quality Operations, Supply Chain and other corporate functions to ensure global consistency, traceability and compliance.

Design, implement and maintain a corporate Quality Agreements management system.

Provide training and technical guidance to local and regional Quality teams on the requirements, structure and management of Quality Agreements.

Drive global harmonization of templates, procedures, and processes related to Quality Agreements within the corporate quality management system.

Develop and present key performance indicators (KPIs) on the status, compliance and cycle times of Quality Agreements to Corporate Quality leadership.

Foster a culture of compliance and shared accountability across the organization through effective and standardized management of Quality Agreements.

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 accommodations may be made to enable individuals with disabilities to perform the essential functions).

• Health Science Bachelor's Degree and/or Master in Farma Industry.
• 2-5 years of experience in similar tasks and/or area.
• High level of English (B2-C1).
• Knowledge of Microsoft Office.
• You have excellent communication skills.
• You have analytical and precision skills.
• You have the ability to work in a team.

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  If you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to apply!

We look forward to receiving your application!

Grifols is an equal opportunity employer.

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