Regulatory Affairs Manager
Descrição da Oferta
Regulatory Affairs Manager
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: [email protected]
Job type: Full-time
Benefits
- Meal voucher/ticket
- Free parking
- Life insurance
- Health insurance
Como Candidatar-se
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