Regulatory Affairs Specialist

Regulatory Affairs Specialist role at Grifols, a global healthcare company. We are a world leader in plasma-derived medicines with a presence in more than 100 countries. The role involves supporting document management, preparation, submission, and follow-up of registration and/or renewal files, as well as any other regulatory documentation.

Requirements

• Bachelor's Degree in Life Sciences field
• 2 years of related technical and/or regulatory experience in pharmaceutical industry or an equivalent combination of education and experience
• Advanced level of English
• User of Microsoft Office tools

Benefits

• Flexible schedule
• Contract of Employment: Permanent
• Flexibility for U Program: Hybrid