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.ResponsibilitiesSupport 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.QualificationsEducation: Bachelor's degree in a Biomedical FieldLanguages: Fluent in Italian and English, other languages will be positively evaluatedExperience: 2+ years in Regulatory Affairs, Quality Assurance, or Product Compliance in the medical device/pharma field.Technical Knowledge: ISO *****, ISO ****, MDR, FDA, CFDA, TGA.Proficient in Microsoft Office Suite.Soft SkillsOrganization & precisionFlexibility/adaptabilityProblem solving & result orientationWorkplace: CID S.p.A., Via Crescentino SNC, ***** SALUGGIA (VC), ItalyContract type: based on the candidate's experienceSalary: based on the candidate's experience"This announcement is open to both genders, in accordance with laws ****** and ******, and to individuals of all ages and nationalities, in accordance with legislative decrees ****** and ******.