Regulatory Affairs Manager Lisboa

Responsibilities

• 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

Schedule: Monday to Friday, from 8:30 am to 5:30 pm.

Apply

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