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.

¿No sabe con seguridad qué habilidades necesitará para esta oportunidad? Simplemente lea la descripción completa a continuación para obtener una idea clara de los requisitos del candidato.

We believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunity fostering an inclusive environment where diversity makes us outstanding.

Responsibilities

-

- Manage product release activities, evaluating technical and documental compliance according to Technical Direction guidelines.

- Participate in the configuration of systems related to product release.

- Coordinate communications with Notified Bodies, reference laboratories and related stakeholders.

- Manage documentation storage, control and retrieval, including externally archived documentation.

- Handle document management quality notifications, ensuring proper tracking and workflow.

- Approve quality notifications after evaluating their impact on batch release and product status.

- Monitor the status of materials affected by quality notifications.





- Coordinate communications with Health Authorities (e.G., AEMPS) and Pharmacy Inspection regarding import/export activities.

- Issue and manage authorizations and official letters required for import/export processes.

- Ensure compliance with applicable regulations such as ISO 13485, IVDR and MDSAP.

- Act as internal auditor and participate in supplier audits.

- Participate in continuous improvement of the Quality Management System.

Qualifications

-

- Bachelor's degree in Engineering, Health Sciences or similar.

- At least 3 years of experience in Quality Assurance or Regulatory Affairs.

- Experience in regulated environments under ISO 13485 and/or IVDR.

- Experience in team management.

- Experience in audits.

- Excellent communication skills.

- Cross‑functional and collaborative work with multiple departments.

- Attention to detail and compliance.

- Analytical ability and technical judgement in impact assessments.

- English level C1.

Benefits

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

Contract of Employment: Permanent.

Location: Parets del Vallès, Spain.

Grifols is an equal opportunity employer.

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. xhfqzwm We are here to help.

Information about Grifols is available at J-18808-Ljbffr

📌 Qa Product Release Section Manager (Parets)
🏢 Grifols
📍 Parets