Life Sciences Job at Grifols – Apply For RA Specialist!
Are you ready to join one of the world’s leading pharmaceutical companies and help shape the future of healthcare? Grifols, a pioneer in plasma-derived medicines, is hiring a Regulatory Affairs Specialist to support global product registration and compliance activities from our Sant Cugat del Vallès location.
- Job Position: Regulatory Affairs Specialist
- Location: Sant Cugat del Vallès
- Contract Type: Permanent
- Area: Technical Operations
About The Company
Founded in 1909, Grifols is a global healthcare leader specializing in plasma-derived therapies and transfusion medicine, serving patients in over 110 countries. With a presence in 100+ markets and a growing workforce, Grifols is committed to advancing human health through innovation, quality, and care.
Job Overview
As a Regulatory Affairs Specialist, you will be responsible for preparing and managing complex submission dossiers, registration renewals, and variations while ensuring regulatory compliance across multiple regions.
Life Sciences Job at Grifols – Key Responsibilities
- Prepare, review, and manage regulatory submissions (CTD/eCTD), ensuring accuracy, compliance, and on-time delivery.
- Liaise with health authorities, affiliates, and third-party partners to track and support regulatory filings.
- Participate in global project teams as the Regulatory Affairs representative.
- Maintain regulatory databases and registration tracking systems.
- Support license updates and product adaptation to current regulations.
- Assist internal departments with regulatory intelligence and documentation.
- Contribute to the development and maintenance of internal SOPs and regulatory procedures.
Life Sciences Job at Grifols – Your Profile
- Bachelor’s degree in Life Sciences or a related field.
- Minimum of 2 years’ experience in a regulatory or technical role within the pharmaceutical industry.
- Strong knowledge of global regulatory requirements and lifecycle management.
- Experience with eCTD/CTD submissions is highly valued.
- Excellent written and spoken English and proficiency with Microsoft Office.
- Detail-oriented, proactive, and a collaborative team player.
Why Join Grifols?
- Hybrid work model: Flexibility through the Flexibility for U program.
- Flexible schedule: Start your day between 7–10 AM (Mon–Thu); Fridays from 8–3 PM.
- Work in a multicultural environment with over 20,000 professionals globally.
- Be part of an organization driven by innovation and a commitment to improving global health.
- Competitive benefits package and long-term career growth.
Keywords: Regulatory Affairs Specialist Spain, Pharmaceutical regulatory jobs Barcelona, eCTD CTD submission jobs, Grifols careers Spain, Regulatory affairs job Sant Cugat del Vallès, Global product registration specialist, Life sciences regulatory careers, CTD lifecycle management
