Bruna Silva Email & Phone Number

Porto, Pt

• Monitor and execute regulatory affairs related to chemical products.• Conduct regulatory analysis of raw materials and evaluate compliance of finished products.• Implement and validate labeling for products.• Create and analyze Safety Data Sheets (SDS).• Respond to customer requests and participate in agreements with customers and suppliers.• Handle product notifications with relevant legal entities, including NEMS, CEFAS, PCN and others.• Ensure compliance with REACH and CLP regulations (EU, UK, KKDIK, UA) for raw materials and finished products.• Collaborate with various departments and entities to maintain regulatory compliance.

• Monitored and executed regulatory affairs related to chemical products.• Conducted regulatory analysis of raw materials and evaluated compliance of finished products.• Evaluated compliance of new products and packaging materials.• Implemented and validated labeling for chemical products.• Created and analyzed Safety Data Sheets (SDS).• Ensured compliance with REACH and CLP regulations and FDA for raw materials and finished products.• Handled product notifications to CHEMTREC.• Responded to customer requests regarding regulatory issues.

• Monitored and executed regulatory affairs related to cosmetic products.• Conducted regulatory analysis of raw materials and evaluated compliance of finished products.• Evaluated compliance of new products and packaging materials.• Approved the release of the finish products to the market.• Provided support in accounting, logistics, and purchasing functions.

• Monitored and executed regulatory affairs related to cosmetic products.• Conducted regulatory analysis of raw materials and evaluated compliance of finished products.• Evaluated compliance of new products and packaging materials.• Managed labeling processes for new products.• Conducted tests on development formulas for new projects.

Vila Nova De Gaia, Porto, Portugal

• Monitored and executed regulatory affairs related to food supplements and medicines at Xamane S.A.• Evaluated compliance of new products and packaging materials.• Managed labeling processes for new products.• Participated in negotiations for Good Manufacturing Practices (GMP) certification for non-certified pharmaceutical laboratories in Dubai and Karachi.• Conducted training sessions on Xamane Laboratory’s food supplements in Portugal and Beirut.

• Provided pharmacological and dermatological advice.• Dispensed prescription and OTC medications.• Managed online sales and order distribution.• Assisted in care facilities.