Senior Regulatory Affairs Specialist (Cosmetic)

Categoria: FMCG (Fast Moving Consumer Goods)
Luogo di lavoro: Italia

Senior Regulatory Affairs Specialist in the cosmetic industry, ensuring compliance with local and international regulations. Trusted technical reference supporting product development and cross‑functional teams, with a strong focus on accuracy, efficiency and regulatory excellence.

The Senior Regulatory Affairs Specialist will be responsible for:

• Ensure regulatory compliance of cosmetic and ideally food and nutraceutical products across EU and non EU markets
• Manage regulatory activities including SDS, CLP labelling, PCN notifications and goods classification for road and sea transport (ADR / IMDG)
• Support technical office activities on product regulations and certifications, including Technical Data Sheets (TDS), product declarations and technical customer support
• Collaborate with Supply Chain on raw material CoA verification and the identification of new suppliers and alternative raw materials
• Interface with Production to manage Bills of Materials (BOM) and production orders, ensuring regulatory and technical alignment
• Monitor evolving regulations, contribute to process improvement and support cross functional teams throughout the product lifecycle

Requisiti: Degree in Pharmacy, Chemistry, Biology, Food Science & Technology, or related fields. 5+ years in regulatory roles. Master's or specialized Regulatory Affairs courses (preferred). Deep knowledge of EMA, AIFA, FDA, EFSA guidelines; EU regulations (cosmetics 1223/2009, food 178/2002 & 1924/2006), GMP/GDP, REACH, CLP. Dossier management and regulatory database expertise. Fluent in English, written and spoken. Degree in Pharmacy, Chemistry, Biology, Food Science & Technology, or related fields. 5+ years in regulatory roles, including 2+ years leading a team. Master's or specialized Regulatory Affairs courses (preferred) Deep knowledge of EMA, AIFA, FDA, EFSA guidelines; EU regulations (cosmetics 1223/2009, food 178/2002 & 1924/2006), GMP/GDP, REACH, CLP. Dossier management and regulatory database expertise. Fluent in English, written and spoken.