Job Title: Healthcare Product Registration Specialist

Overview
We are seeking a Healthcare Product Registration Specialist to join our Regulatory Affairs team. This role focuses on managing regulatory registrations, submissions, and related documentation for medical devices, ensuring regulatory compliance and timely market access.

About the Role
- Lead end-to-end regulatory registrations and submissions for healthcare products.
- Prepare, maintain, and organize technical documentation, archives, and regulatory dossiers.
- Communicate with government authorities to obtain and maintain approvals as required.
- Collaborate with cross-functional teams including product development, quality, and marketing to ensure ongoing regulatory compliance throughout the product lifecycle.
- Monitor regulatory developments and interpret regulations to inform labeling, packaging, and registration strategies.
- Contribute to strategic planning and planning of registration activities and lifecycle management.
- Produce reports and maintain transparent documentation for stakeholders.
- Support education and training on regulatory requirements within the organization.

Required Skills
- Documentation
- CE marking
- Registration
- Regulatory Submissions
- Regulations
- Regulatory Affairs
- Medical Devices
- Government
- Product Development
- Planning
- Strategic Planning
- Reporting
- Archives
- Leadership
- Presentation Skills
- Education
- Italian

What We Offer
- A collaborative and professional work environment
- Opportunities for professional growth and development
- Flexible work options and a focus on work-life balance

How to Apply
Please submit your resume and a brief cover letter outlining your relevant experience.