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 fieldTechnical Knowledge: ISO 13485, ISO 9001, MDR, FDA, CFDA, TGAProficient in Microsoft Office SuiteSoft SkillsOrganization & precisionFlexibility / adaptabilityProblem solving & result orientationWorkplaceCID S.p.A., Via Crescentino SNC, 13040 SALUGGIA (VC), ItalyContract typeBased on the candidate’s experienceSalaryBased on the candidate’s experienceThis 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.
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