A global healthcare leader is seeking a Nucleic Acid Testing (NAT) Regulatory Affairs Specialist for their Diagnostic Regulatory Affairs department in Sant Cugat del Vallès, Spain. The ideal candidate will hold a Bachelor's Degree in Health Sciences and have experience in regulatory affairs within the pharmaceutical industry. Responsibilities include preparing technical documentation, coordinating regulatory submissions, and defining regulatory requirements. The role also demands fluency in Spanish and English. Join a company that values diversity and offers a supportive working environment.#J-18808-Ljbffr