Job Title

About Indorama Ventures: Indovinya It's a top producer company of chemical intermediates and surfactants. As producers of solutions used for home and personal care, crops, coatings, energy and resources and other applications, we are present in the daily lives of millions worldwide. Through our increasingly sustainable chemistry, designed to meet the needs of each of our customers carefully, we want to transform our operations and products into something increasingly relevant for the planet. Position Overview Accountable for ensuring regulatory compliance of Indovinya' s products commercialized in North America (USA, Canada and Mexico) according to regulations related to chemical registration and application of use (e.g., FDA, FIFRA). Oversees compliance with the Toxic Substances Control Act (TSCA) for all US sites. Responsible for maintaining TSCA registrations, ensuring ongoing compliance, and providing expert advice on North America chemical regulations. Required Skills Bachelor's degree is required on Chemistry, Biology, Chemical Engineering or Agricultural Engineering. 5+ years of experience in global regulations and governance within chemical industry. At least 3 years of experience in TSCA requirements and history preparing LVE/PMN submissions. Knowledge of chemistry and manufacturing processes. Experience working with SAP EHS modules and SVT Advanced English (C1) Main Responsibilities Manage, prepare and submit all TSCA Pre-Manufacture Notifications (PMN) submissions to US EPA and follow-up with US EPA to shepherd submissions to successful completion; and similar for New Substance Notifications (NSN) to Canada. Prepare TSCA Import certifications and participate in TSCA advocacy issues where necessary. Chemical Data Reporting (CDR) to the U.S. Environmental Protection Agency (EPA) for all US sites. Stay informed of the status of chemicals being reviewed by US EPA for TSCA enforcement and keep current with any changes to TSCA regulations. Prepare RACI and procedures for all North America Compliance related processes. Conduct a regulatory evaluation for all products prospected for North America related to chemical registration (e.g., DSL, NDSL, TSCA) and application of use. INCI Submissions for PCPC. FDA evaluations and FDA registrations for products marketed in North America. Keep all the records in our repository to ensure traceability of the data related to North America. What We Offer: A dynamic, global environment where you'll have the opportunity to shape organizational strategy Career growth and development opportunities Competitive salary and additional benefits