Requirements: ➡ Excellent understanding of medical devices to ensure our products fulfill all regulatory directives; ➡ Compile, review, submit, and follow up any applications for use \- CE marking, FDA, ISO 13485, INFARMED, UKCA, MDSAP; ➡ Registration of medical devices in various countries ➡ Actively research and analyze scientific data; ➡ Cooperate on new projects; ➡ Perform and manage audits; ➡ Collaborate on strategic planning together with top management; ➡ Work closely with partners, consultants, manufacturers, scientists, health professionals, and others; ➡ Lead and manage regulatory audits; ➡ Liaise with regulatory officials and consultants; ➡ Good communication and interpersonal skills; ➡ Proactive and action maker; ➡ Proficient English (written and spoken). ⠀ What we offer: ✅ Positive work environment ✅ Salary commensurate with proven experience ✅ Work\-related training ✅ Health insurance and other employee benefits ✅ High\-responsibility position ✅ Integration into a growing company ✅ Full\-time job ⠀ Schedule: Monday to Friday, from 8:30 am to 5:30 pm. ⠀ Apply now! Send your resume to: p.figueiredo@astrolabe\-medical.com Tipo de oferta: Integral/Full\-time Benefícios: * Cartão/Ticket refeição * Estacionamento gratuito * Seguro de vida * Seguro saúde