International Regulatory Affairs Specialist

General Description:

The International Regulatory Affairs Specialist is responsible for ensuring that products comply with international regulatory requirements across multiple regions. This role supports product registration, regulatory strategy, and compliance activities to enable global market access. This includes reviewing product chemistry, toxicology, and efficacy data, as well as verifying the accuracy and integrity of supporting scientific research. This role requires close collaboration with sales and marketing to support compliant product strategies and effectively prioritize and manage related projects.

Regulatory Strategy & Complianc

• eSupport development and execution of global regulatory strategies for product registration and lifecycle managemen
• tInterpret and apply regulations across multiple regions
• .Identify regulatory risks and opportunities, developing strategies to mitigate risks and enhance success rates

.
Registrations & Submissio

• nsEnsure timely preparation and submission o
• f:Regulatory dossie
• rsRegistration applications and amendmen
• tsData compensation documentati

on
Cross-Functional Collaborat

• ionPartner wi
• th:R&am
• p;DProduct stewards
• hipMarketing and commercial te
• amsProvide regulatory guidance f
• or:New product developm
• entLabel claims and position
• ingMarket entry strateg

ies
Project Manage

• mentManage multiple regulatory projects simultaneo
• uslyEstablish priorities and ensure timely completion of delivera
• blesTrack regulatory milestones and maintain internal sys

tems
Stakeholder Communic

• ationCommunicate regulatory requirements and compliance expectations directly with customers, providing guidance on product use, labeling, and registration status across global mar

kets.
Qualific

• ationsBachelor’s degree in life science, environmental science, chemistry or related disci
• pline.5 years regulatory experience in specialty chemical industry including product stewardship, USEPA and international regulatory processes and requirements. e.g. FIFRA, Biocidal Products Regulation, Plant Protection Regulation, OECD, REACH
• , CLP.Hands‑on experience preparing and managing regulatory submissions for multiple international ma
• rkets.Occasional domestic and international travel req
• uired.Fluency in Spanish, a plus but not req
• uired.Proficiency in MS Office (Word, Excel, PowerPoint, Ou