At Roche you can show up as yourself, embraced for the unique qualities you bring. Formulate sound regulatory submission plans to secure market access globally. Health Authority & Compliance Frameworks: Apply knowledge of general regulations (e.g., Champion continuous improvement and explore new digital tools or automated workflows to drive efficiency. VACC Leadership & Agile Mindset: University degree (Bachelor’s or Master’s) in Life Sciences, Biotechnology, Biomedical Engineering, Data Science, or a related field (or equivalent practical experience). Professional

Experience:
1+ years of relevant experience within Regulatory Affairs, Quality Assurance, R&D;, or Clinical Operations in healthcare or life sciences. Digital & IT Fluency: Proficiency in MS Office and Electronic Document Management Systems (EDMS/RIMS). Fluency in English (both written and spoken), with the ability to communicate regulatory concepts clearly across diverse teams. Hands‑on experience with IVD (In‑vitro Diagnostics) or Medical Device regulations (EU IVDR 2017/746, US FDA 510(k)/PMA, etc.).



Familiarity with international quality standards (e.g., Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life‑changing healthcare solutions that make a global impact. We believe it's urgent to deliver medical solutions right now – even as we develop innovations for the future. And we believe that good business means a better world. We commit ourselves to scientific rigor, unassailable ethics, and access to medical innovations for all. We are many, working as one across functions, across companies, and across the world.

📌 Regulatory Affairs Officer (España)
🏢 Roche
📍 España