Regulatory Affairs Specialist (Specialty Chemicals & Protective Materials)

We are seeking an experienced Regulatory Affairs professional to support a global specialty chemicals and protective materials manufacturer as it expands its product portfolio into new international markets. This individual will serve as the regulatory lead for a multi‑region commercialization initiative, helping leadership clear country‑specific compliance requirements, identify and close gaps, and enable on‑time market entry across the U.S., EU, and other global markets. The ideal candidate brings deep Regulatory Affairs expertise in chemical and formulated‑product compliance, a working command of international regulatory frameworks for industrial chemical products, and the ability to operate in an ambiguous, fast‑moving environment while advising both executive leadership and cross‑functional execution teams. This is a highly consultative, execution‑oriented role requiring hands‑on experience with country‑specific chemical regulations, restricted‑substance requirements, product registrations and certifications, hazard classification and labeling, and the regulatory dimensions of entering new geographic markets. Product Scope Regulatory support spans the company's portfolio of specialty chemical and protective‑materials product lines, including: Protective coatings and chemically resistant linings Cold‑applied and pressure‑sensitive tapes Sealants, waterproofing compounds, and joint‑sealing materials Cable‑management, locating/tracer, and water‑blocking products Other formulated industrial chemical products These serve end markets such as waterproofing, chemical containment, commercial construction and infrastructure, utilities, telecom, and oil & gas. Key Responsibilities Serve as a Regulatory Affairs subject matter expert for the geographic expansion program, supporting product‑level regulatory clearance across target markets. Evaluate country‑specific regulatory requirements for chemical‑based products including allowable chemical compositions, restricted substances, registration, certification, labeling, and commercialization requirements. Make and document substance vs. article‑type determinations and registration strategies under frameworks such as REACH/CLP, and assess applicability of restricted‑substance regimes (e.g., RoHS, POPs) on a product‑by‑product basis. Manage country and regional certification and conformity pathways for example EU construction‑product and CE requirements, and national schemes across the EU, Middle East, North America, and Asia (e.g., SASO/SABER, NOM/STPS, WHMIS, BIS, and applicable GB standards). Author and coordinate Safety Data Sheets, GHS/CLP hazard classifications, and multi‑language label and documentation translations to meet each market's requirements. Identify regulatory gaps, risks, and dependencies that affect launch timing, and translate them into clear critical‑path items for the program plan. Advise leadership on regulatory considerations tied to international market strategy, legal‑entity structure, and product import/commercialization pathways. Support the regulatory dimensions of product transfers, and supplier/manufacturing transitions where applicable. Collaborate cross‑functionally with commercial, operations, legal, quality, supply chain, and R&D teams, and provide regular status against program milestones. Support development of scalable, repeatable regulatory processes and frameworks as the company expands into additional markets. Monitor evolving global chemical and product regulations and assess their impact on the portfolio. Required Qualifications Proven Regulatory Affairs experience with industrial chemical, coatings, adhesives/tapes, sealants, or other formulated/specialty‑materials products. Demonstrated command of international chemical regulatory frameworks (e.g., REACH/CLP, RoHS, POPs) and country‑specific product registration, certification, and labeling requirements. Experience authoring or directing SDS preparation and GHS/CLP hazard classification. Track record supporting multi‑market product launches or registrations on defined timelines. Ability to operate independently in an ambiguous, evolving environment and to advise executive leadership on both strategic and operational regulatory matters. Strong cross‑functional collaboration skills across commercial, operations, legal, quality, and R&D. Preferred / Nice to Have Experience with construction‑product regulation, electrical/electronic product compliance, or related conformity standards. M&A regulatory due‑diligence experience and exposure to product/manufacturing transfers. Familiarity with MedTech or medical‑device regulatory frameworks (e.g., ISO 13485, EU MDR, FDA)