NAT Regulatory Affairs Specialist — Flexible Hours

Grifols, S.A; Sant Cugat del Vallès; Presencial; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

A globally recognized healthcare company in Spain is seeking a Regulatory Affairs Specialist. You will manage technical documentation, product registration, and compliance with regulations. Ideal candidates will have a Bachelor's in Health Sciences and experience in the pharmaceutical industry, alongside advanced Spanish and English skills. Enjoy a supportive and inclusive work environment with flexible schedules and a commitment to your professional development.

Servicios

Flexible schedule

Benefits package

Permanent contract

Formación

• Experience in RRAA within the pharmaceutical industry.
• Advanced level of Spanish and English (C1).

Responsabilidades

• Prepare and send registration and renewal dossiers.
• Prepare technical documentation based on R&D inputs.
• Coordinate documents for regulatory submissions.
• Define regulatory requirements for products.
• Prepare official responses to Health Authority questions.

Conocimientos

Analytical skills

Attention to detail

MS Office proficiency

Educación

Bachelor's Degree in Health Sciences

Descripción del empleo

A globally recognized healthcare company in Spain is seeking a Regulatory Affairs Specialist. You will manage technical documentation, product registration, and compliance with regulations. Ideal candidates will have a Bachelor's in Health Sciences and experience in the pharmaceutical industry, alongside advanced Spanish and English skills. Enjoy a supportive and inclusive work environment with flexible schedules and a commitment to your professional development.