Regulatory Affairs Jobs at Grifols Spain
Are you searching for high-impact Regulatory Affairs jobs in Europe with a global healthcare leader? This permanent opportunity at Grifols offers life science professionals the chance to work at the forefront of regulatory compliance, international product registrations, and healthcare innovation. Located in Spain, this role is ideal for professionals seeking long-term growth in regulatory affairs specialist careers within a world-class pharmaceutical organization.
About the Company
Grifols is a global healthcare company founded in 1909 and a world leader in plasma-derived medicines and transfusion solutions. Operating in more than 110 countries, Grifols employs over 20,000 professionals worldwide. Known for innovation, diversity, and ethical business practices, jobs at Grifols offer meaningful careers that directly impact global health.
Regulatory Affairs Job Details:
- Job Title: Regulatory Affairs Specialist
- Location: Sant Cugat del Vallès, Spain
- Job Type: Permanent · Full-time · Hybrid
- Job ID: 537456
- Area: Technical Assistance
Role Mission
Support document management, preparation, submission, and follow-up of regulatory dossiers, including registrations, renewals, and variations, ensuring compliance with global regulatory requirements and timelines.
Key Responsibilities
- Prepare, review, submit, and track regulatory dossiers (registrations, renewals, variations).
- Communicate with affiliates, external partners, and Health Authorities.
- Represent Regulatory Affairs on cross-functional project teams.
- Adapt product licenses to current regulatory requirements.
- Maintain regulatory tracking systems and documentation.
- Support internal departments and affiliates with regulatory information.
- Develop and maintain regulatory policies and procedures.
Qualifications
- Bachelor’s degree in Life Sciences or related field.
- ~2 years regulatory or pharmaceutical industry experience (preferred).
- Experience with global regulatory requirements and product registrations (preferred).
- Experience with CTD/eCTD submissions and dossier lifecycle management (highly valued).
- Advanced English proficiency.
- Proficient in Microsoft Office.
- Strong attention to detail, communication, teamwork, and initiative.
What Grifols Offers for Regulatory Affairs Jobs
- Permanent employment with a global healthcare leader.
- Hybrid work model (U Program).
- Flexible working hours (Mon–Thu flexible start; Fri 8–3).
- Competitive benefits package.
- Inclusive, diverse, and development-focused work environment.
