Regulatory Affair Associate - Cosmetic & Skincare in New Jersey

Responsibilities:

• Responsible for generating ingredient lists, quantitative formulas, exploded formulations (Decks), as well as multiple document types.
• Generate raw material regulatory statement: origin, cruelty-free, BSE & TSE, heavy metal, impurity, REACH-Compliance, global & regional compliance, food allergen, fragrance allergen, nitrosamine-free, vegan, gluten-free, nano, CMR, etc.
• Generate Finished Good SDS.
• Generate a global compliance report and review the report against jurisdictional compliance.
• Review formulas either using the software system or the PCPC International Raw Material Database.
• Responsible for gathering portions or all of the PIFs (Product Information Files) for the EU registration.
• Communicate with Vendors/suppliers for RM documents and follow up on requests with vendors.
• Communicate with customer service personnel and EWL chemist to give project status...