Regulatory Affairs Specialist

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.