Te gustaría unirte a un equipo internacional que trabaja para mejorar el futuro del sector de la salud? ¿Grifols es una compañía general 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 looking for an Immunohematology (IH) / Operations Regulatory Affairs Specialist to join Diagnostic Regulatory Affairs department. The RRAA Specialist will be responsible for the preparation of technical documentation, submission, following up and controlling of product registration and/or renewal, variations dossiers, as well as giving support to Regulatory transversal project.
Coordinate the preparation of the documents needed for regulatory submissions with R&D;, manufacturing and QA departments.
Review and assess regulatory impact on product or manufacturing changes. Revise, approve and/or coordinate packaging material. Review technical documents to ensure coherence and compliance with regulatory requirements.
Assist commercial teams with regulatory documentation for tenders and customers You have a Bachelor's Degree in Health Sciences or engineering. You have been working in RRAA or technical departments within the pharmaceutical industry. You have Advanced level of Spanish and English (C1) and of MS Office (Excel).
Hybrid Model
Monday-Thursday 7-10 to 16-19h and Friday 8-15h. (Contract of Employment: Permanent position Ubicación: SPAIN : España : Sant Cugat del Valles:[[cust_building]]