MSD in Spain is seeking a Regulatory Affairs Specialist to join our Regulatory Affairs team, driving lifecycle management for Oncology and Vaccines. You will work with local, regional, and integral partners and engage with authorities such as AEMPS to ensure compliant and timely patient access to innovative therapies. The ideal candidate has a Life Sciences degree, 1–2 years in pharma regulatory affairs, fluent Spanish and English, and strong organizational skills. #J-18808-Ljbffr
📌 Regulatory Affairs Specialist: Oncology (España)
🏢 Msd
📍 España
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