Regulatory Affairs Specialist
hace 4 semanas
We are committed to fostering an inclusive environment that values diversity and promotes equal employment opportunities.
As a world leader in plasma-derived medicines, we are seeking a highly skilled Regulatory Affairs Specialist to join our team.
Key Responsibilities:- Prepare and submit technical documentation for product registration and renewal.
- Coordinate with R&D, manufacturing, and QA departments to ensure regulatory compliance.
- Define regulatory requirements for products and adapt licenses to current regulations.
- Manage the delivery of product samples and labels related to product registration processes.
- Review and assess regulatory impact for product or manufacturing changes.
- Bachelor's Degree in Health Sciences or Engineering.
- Experience in R&D or technical departments.
- Advanced level of Spanish and English (C1) and of MS Office (Excel).
- Analytical skills, attention to detail, and ability to summarize and evaluate.
- A challenging and rewarding career in a critical function.
- A flexible schedule with Monday-Thursday 7-10 to 16-19h and Friday 8-15h.
- A comprehensive benefits package.
- A permanent position with opportunities for growth and development.
We look forward to receiving your application and welcoming you to our team at Grifols.
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