Clinical QA Trainee

To successfully perform this job, a person must be able to carry out the responsibilities 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.

• You are currently pursuing a Degree or Master's in Pharmaceutical Industry, Pharmacy, Biology, Biotechnology, Health Sciences, or related fields.
• You have complemented your training with a specialization in Clinical Research, Clinical Trial Monitoring, Quality Systems, or related disciplines.
• You are proficient in the Microsoft Office suite, especially Excel and Word, for the analysis, monitoring, and management of information.
• Valuable previous experience or knowledge in clinical document management tools (e.g., electronic eTMF) or other similar platforms.
• You have an advanced level of English (C1) that allows you to move comfortably in international environments and work with technical documentation.

• Compensation: Study assistance and company canteen.
• An opportunity to train in a highly regulated and international environment.
• To join a multidisciplinary team, with real opportunities to learn and grow in the pharmaceutical industry.

Being part of Grifols means the opportunity to work in an international environment where equal opportunities are promoted.

It means the opportunity to develop professionally, have continuous training, and integrate into a team of professionals where each individual's contribution counts. Our commitment is to maintain an environment that fosters the professional development of our employees in a good work atmosphere.

Grifols' human capital is key to both the development of activities and the company's expansion process.

If you are interested in growing with us and your profile fits this professional opportunity, send us your CV!

Location: SPAIN : España : Sant Cugat del Valles:[[cust_building]]

Learn more about Grifols

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.

Join Grifols!

At Instituto Grifols S.A, we require the incorporation of a Trainee for the Clinical Quality Assurance department.

• You will collaborate in the administrative and operational tasks of the Process Control group.
• You will provide support in the management of supplier qualification.
• You will review clinical trial documentation and participate in the associated quality controls.
• You will prepare quality metric monitoring reports.
• You will participate in the organization and maintenance of clinical archives, including electronic TMF systems.
• You will communicate with other departments to coordinate cross-functional tasks.
• You will collaborate in the administrative and operational tasks of the QA Audits group.
• You will provide support in the preparation, execution, and follow-up of the audits performed.