¿Te gustaría unirte a un equipo internacional que trabaja para mejorar el futuro del sector de la salud? ¿Quieres contribuir a mejorar la vida de millones de personas? Grifols es una compañía global del sector de la salud que desde 1909 mejora la salud y el bienestar de las personas en todo el mundo. Somos líderes en medicamentos hemoderivados y medicina transfusional y desarrollamos, producimos y comercializamos medicamentos, soluciones y servicios innovadores en más de 110 países y regiones.
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.
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 Regulatory Affairs Specialist like you.
What your responsibilities will be
1. Prepare and send the registration and/or renewal and/or changes/variations dossiers of the relevant products.
2. Prepare technical documentation based on the R&D inputs.
3. Coordinate the preparation of the documents needed for regulatory submissions with R&D, manufacturing and QA departments.
4. Define the regulatory requirements for the products.
5. Prepare and send official responses to any Health Authority questions.
6. Review and assess regulatory impact for product or manufacturing changes.
7. Adapt licenses to current regulations.
8. Manage/coordinate the delivery of product samples or labels related with product registration/renewal/change processes.
9. Revise, approve and/or coordinate packaging material.
10. Review technical documents to ensure coherence and compliance with regulatory requirements.
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).
11. You have a Bachelor's Degree in Health Sciences or engineering.
12. You have experience in RRAA or technical departments within the pharmaceutical industry.
13. You have analytical skills, attention to detail, and ability to summarize and evaluate.
14. You have Advanced level of Spanish and English (C1).
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.
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!
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.