Manager, Regulatory Intelligence

Zoetis

. Own and lead assigned global surveillance workstreams, independently monitoring, interpreting, and communicating evolving regulatory requirements .

Posted 10/22/2026full-timeRemote • United StatesMid-LevelSenior💰 $120,000 - $180,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Regulatory Affairs with a strong focus on managing regulatory deliverables, leading cross-functional teams, and interpreting evolving regulatory requirements. Proficient in utilizing regulatory intelligence systems and AI technologies to enhance compliance and communication processes.

Highest-signal resume keywords

Regulatory Affairs ExperienceRegulatory Intelligence SystemsCross-Functional Team LeadershipFDA InteractionAI Software Proficiency

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Regulatory ComplianceRegulatory Deliverables ManagementRisk AssessmentGMP InspectionChemical Regulations UnderstandingSustainability Regulations KnowledgePortfolio ManagementEPR ReportingQuality AssuranceSubject Matter Expertise

Soft Skills

CommunicationCollaborationLeadershipProblem-SolvingStakeholder Engagement

Tools & Technologies

Regulatory Intelligence PlatformsAI TechnologiesGenAI SoftwareCompliance Tracking ToolsDigital Tools for Regulatory Intelligence

Industry Keywords

Pharmaceutical RegulationsAnimal Health Product LawsChemical Substances RegulationsBio Pharmaceutical ResearchGlobal Health Authorities

About the role

Key responsibilities & impact

Own and lead assigned global surveillance workstreams, independently monitoring, interpreting, and communicating evolving regulatory requirements
Oversee monitoring across compendial changes, chemical requirements, pharmaceutical and non-pharmaceutical packaging, diagnostics, medical devices, and GMP/Environmental inspectional activities
Coordinate cross-functional impact assessments with EHS, VMRD, Quality, Global Manufacturing, Public Affairs, and Legal
Ensure assessments are completed, compliance plans are documented, and actions are tracked to closure
Lead development and distribution of regulatory intelligence newsletters, regulatory watch notifications, and ad hoc query responses
Review and quality-check RI communication outputs produced by team members
Coordinate company responses to draft guidance, standards, and consultations
Manage SME engagement, consolidate inputs, and ensure submissions reflect a clear, defensible company position
Represent the company in relevant industry associations and regulatory forums
Manage EPR reporting data submissions through timely and accurate filing with state and/or national programs
Act as a subject matter expert on new and emerging regulations or requirements when needed
Coordinate external consultant activities, including scope definition, budget review and approval, and ongoing liaison
Serve as primary point of contact for specific internal stakeholder groups for RI-related inquiries
Interpret regulatory compliance trends, assess emerging risks, and prepare action plans and briefings for Governance forums
Contribute to the design, documentation, and sustainability of RI processes and SOPs
Champion AI-enabled regulatory intelligence platforms and contribute to selection, piloting, implementation, and training on RI-specific digital tools

Requirements

What you’ll need

Bachelor’s degree in a scientific discipline (e.g., life sciences, pharmacy, regulatory affairs, or related field)
Minimum 5 years of experience in Regulatory Affairs or related field
Demonstrated track record of independently managing regulatory deliverables and leading cross-functional workstreams or acting as Subject Matter Expert within a cross-functional team
Experience with regulatory intelligence systems or tools required at this level
Previous interactions with FDA, USDA, or other US authorities strongly preferred
Experience in a Regulatory Intelligence function preferred
General knowledge of (bio) pharmaceutical research and development, authorization and post-marketing compliance of medicinal products
Good understanding of CMC preferred
Experience as an active participant or representative in industry associations, with demonstrated contribution to working groups or policy discussions
Working knowledge of animal health product laws, regulations, and the regulatory policy-making process
Understanding of chemical substances laws and regulations
Familiarity with sustainability and packaging regulations, including US State EPR reporting frameworks and PRO data submission requirements
Experience managing a portfolio of regulatory liaison activities directly with Global Health Authorities
Hands-on experience with AI software and GenAI technology applied to regulatory intelligence workflows
All applicants must possess or obtain authorization to work in the US for Zoetis; individuals requiring sponsorship must disclose this fact

Benefits

Comp & perks

Short-term incentive compensation
Long-term incentives
Healthcare and insurance benefits beginning on day one
401K plan with a match and profit-sharing contribution from Zoetis
4 weeks of vacation