Assistant Manager Regulatory Affairs

As an Assistant Manager in Regulatory Affairs at our Haridwar factory, your primary role will be to review product formulations in accordance with Indian FDA (Cosmetics & Ayurvedic) regulation, EU Cosmetics Regulation (EC 1223/2009), US FDA, ASEAN, and GCC guidelines. Your responsibilities will include preparing and maintaining regulatory dossiers such as Product Information Files (PIF) and safety assessments to meet export requirements. You will also be tasked with reviewing product labels, ingredient lists, and claims to ensure compliance with country-specific regulations. Additionally, you will be responsible for preparing Product Safety Data Sheets as per export regulations and staying updated on changing regulations to inform stakeholders. Collaboration with the Design team for label development, as well as coordination with R&D, Quality Assurance, and RM procurement teams for regulatory needs, will be crucial. Your role will also involve providing regulatory input to R&D for new product development to ensure global market acceptance, along with maintaining records, documentation, and regulatory databases for all export product formulations. Qualifications required for this role include a Master's degree in Pharmacy or Chemistry, knowledge of global cosmetic regulations, export documentation processes, familiarity with regulatory portals, and international submission formats. Additionally, a minimum of 5-7 years of experience in Technical Regulatory Affairs, preferably in the Ayurvedic, Cosmetics, or Personal Care sector, is essential. Join our team to contribute to regulatory compliance and product development in the Personal Care - Cosmetics/Ayurvedic industry at our Haridwar factory.,