Regulatory Affairs Specialist

Overview

CID S.P.A., a medical device manufacturing and selling company, is looking for a full-time Regulatory Affairs Specialist to join our Regulatory Affairs Team (On-site, Italy). The resource, reporting directly to the CSRO, will support regulatory processes and compliance activities within a structured and international environment.

Responsibilities

• Support registrations and approvals for commercialization of medical devices (new, renewals, updates, modifications).
• Collaborate with distributors, consultants, and competent authorities worldwide.
• Review labels and packaging in line with current regulations.
• Ensure proper documentation management, submission, and archiving.
• Support internal departments in preparing technical regulatory documentation.

Qualifications

• Education: Bachelor’s degree in a Biomedical Field
• Languages: Fluent in Italian and English, other languages will be positively evaluated
• Experience: 2+ years in Regulatory Affairs, Quality Assurance, or Product Compliance in the medical device / pharma field
• Technical Knowledge: ISO 13485, ISO 9001, MDR, FDA, CFDA, TGA
• Proficient in Microsoft Office Suite

Soft Skills

• Organization & precision
• Flexibility / adaptability
• Problem solving & result orientation

Workplace: CID S.P.A., Via Crescentino SNC, 13040 SALUGGIA (VC), Italy

Contract type: based on the candidate’s experience

Salary: based on the candidate’s experience

This announcement is open to both genders, in accordance with laws 903 / 77 and 125 / 91, and to individuals of all ages and nationalities, in accordance with legislative decrees 215 / 03 and 216 / 03.