14 oct
|
Grifols
|
Játiva
Grifols, S.A is seeking a Regulatory Affairs professional to manage complex regulatory submissions (CMC) and oversee change requests for multiple production sites. You will coordinate with Health Authorities and affiliates to ensure timely regulatory reporting and maintain regulatory strategy processes.
Requirements include a Health Sciences degree, experience in RRAA within pharma, and fluency in Spanish and English (C1).
📌 Diagnostic Regulatory Affairs Ih (Játiva)
🏢 Grifols
📍 Játiva