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;
➡ Actively research and analyze scientific data;
➡ Cooperate on new projects;
➡ Training management; SHST management and others for QMS management;
➡ 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).
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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
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Schedule: Monday to Friday, from 8:30 am to 5:30 pm.
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Apply now! Send your resume to: p.figueiredo@astrolabe-medical.com
Tipo de oferta: Integral/Full-time Benefícios: