OverviewSi cree que es el candidato ideal para la siguiente oportunidad, envíe su solicitud después de leer la descripción completa.Join Roche as an International Regulatory Affairs Professional to drive regulatory excellence for integral IVD/MD instruments and software. You will collaborate with R&D;, Quality, and Clinical teams to shape submissions, stay ahead of regulatory developments, and support product lifecycle management. This role offers meaningful global impact through enabling access to healthcare and advancing medical solutions. You’ll thrive in a collaborative, innovative environment and help define the future of regulatory strategy at Roche.Compensaciones / Beneficioscompetitive compensation and benefits packageprofessional development and growth opportunitiesResponsabilidadesLead and support regulatory strategies for global IVD/MD instrument and software submissionsEnsure compliance with international regulatory requirements and standardsCollaborate with cross-functional teams to drive regulatory initiativesProvide regulatory guidance to support product development and lifecycle managementStay informed on evolving regulatory trends and implement best practicesRequisitos principalesBachelor’s Degree in Life Sciences, Regulatory Affairs, or related field5 to 7 years of experience in Regulatory Affairs (Regulatory, R&D;, Quality and/or Clinical)Deep knowledge of global regulatory requirements, guidelines, and procedures xhfqzwm for IVD instruments & softwareStrong organizational and communication skillsAbility to multitask and manage multiple projectsSelf-motivated with ability to work independentlyExperience in IVD instrument and/or software developmentcollaborationcommunicationself-motivationglobal regulatory requirements, guidelines, and proceduresIVD instruments & softwareregulatory submissions

📌 Abogado/A De Regulación Digital (Gracia)
🏢 Alexion
📍 Gracia