Company Description
Power Dream is a dedicated participant in the global Energy Curing industry, specializing in oligomers, monomers, and additives. With over 20 years of experience, we prioritize innovation, eco-friendliness, substance, and responsibility. Our goal is to introduce cutting-edge technologies to diverse markets including graphic arts, coatings, nail care, adhesives, and electronics. We value exceptional customer care and attention and strive to address our customers' unique needs through value-added service.
Role Description
This is a remote/ hybrid role
Responsibilities:
- Regulatory Implementation: Leads projects for the implementation of GHS regulatory standards in accordance with OSHA 2012 and WHMIS 2015.
- SDS Systems: Implements new SDS authoring systems, templates, and labels.
- EPA Compliance: Handles the preparation and submission of EPA Chemical Data Reporting (CDR), facilitates EPA Section 11 site inspections, and manages compliance with EPA TSCA Sections 4, 5, 6, 8.12, and 13.
- FDA Compliance: Reviews FDA compliance and prepares documentation, including FCN dossier support and usage reviews.
- Consultant and Agency Liaison: Coordinates with external regulatory consultants, legal counsel, governmental agencies, and participates in chemical trade association councils.
- Regulatory Documentation: Reviews new and existing chemicals for market feasibility, evaluates market strategies, and advises on market rights.
- System Management: Manages the integration, maintenance, and testing of the SAP ERP system and WERCS Authoring.
- Reporting and Documentation: Prepares and submits U.S. Pre-Manufacturing Notifications (PMNs) and Canadian New Substance Notifications (NSN), along with regulatory reports such as Chemical Weapons reporting and TSCA Section 8.
- Training and Support
