Clinical QA Systems and Documentation Specialist

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.

**Summary** **:**

Responsible for the life cycle management of R&D and Clinical documents according to company SOPs. Participate in the implementation of new systems or improvements to existing systems. Administer the clinical trial documentation system in compliance with regulations and procedures so that documents are retrievable in a timely and efficient manner. Responsible for maintaining and developing training profiles and documentation for Clinical departments.

**Primary responsibilities for...