Regulatory Affairs Manager Vialonga

Regulatory Affairs Manager
Lisboa
Vialonga, Lisboa, Portugal

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).
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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. -

Tipo de oferta: Integral/Full-time

Benefícios:

• Cartão/Ticket refeição
• Estacionamento gratuito
• Seguro de vida
• Seguro saúde