VP, Regulatory & Public Affairs

The Center for Aquaculture Technologies (CAT)

. Lead CAT's global regulatory strategy for Genome Editing and other advanced technology programs across priority markets .

Posted 10/2/2026full-timeRemote • United StatesLead💰 $210,000 - $230,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in developing and executing regulatory strategies for Genome Editing and advanced technologies, with a strong focus on stakeholder engagement and market access. Possesses a deep understanding of regulatory frameworks and the ability to translate complex scientific concepts into actionable insights for diverse audiences.

Highest-signal resume keywords

Regulatory Strategy DevelopmentGenome Editing ExpertiseStakeholder EngagementPublic Affairs StrategyRegulatory Affairs Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Regulatory Pathway DefinitionEvidence Requirement AnalysisMarket Access StrategyRegulatory Intelligence BuildingScientific CredibilityCommercial UnderstandingBiotechnology RegulationGenetics and Genomics KnowledgeAnimal Health RegulationPublic Policy Expertise

Soft Skills

Excellent Communication SkillsInfluencing SkillsPragmatic ApproachEntrepreneurial MindsetStrong Judgment

Industry Keywords

AquacultureLife SciencesBiotechnologyAnimal BreedingHighly Regulated IndustryInternational Regulatory StrategyEmerging TechnologiesStakeholder MappingRegulatory FrameworksScience-Based Dialogue

About the role

Key responsibilities & impact

Lead CAT's global regulatory strategy for Genome Editing and other advanced technology programs across priority markets
Define regulatory pathways, priorities, evidence requirements, milestones and decision points for active and future programs
Develop and execute CAT's Public Affairs strategy, including stakeholder mapping, engagement priorities and key messages
Build trusted relationships with regulators, policymakers, government agencies, industry organizations, certification bodies, clients and other influential stakeholders
Represent CAT in relevant regulatory, policy, scientific and industry forums
Monitor and interpret emerging regulatory frameworks, policies and precedents
Promote credible, transparent and science-based dialogue around Genome Editing and its responsible application in aquaculture
Integrate regulatory, market-access and stakeholder considerations into R&D, technology and commercial decision-making
Partner with Commercial and Business Development teams to support market access, client adoption and commercialization
Advise the CEO and executive leadership on regulatory developments, policy trends, stakeholder considerations and associated business opportunities and risks
Build CAT's regulatory intelligence and institutional knowledge, including regulatory precedents, submissions, evidence and stakeholder engagement history
Coordinate external regulatory, legal, scientific and public-affairs expertise where jurisdiction-specific or specialist support is required
Build a scalable Regulatory & Public Affairs capability as CAT's technology portfolio and commercialization activities expand
Initially report directly to the CEO and work closely with scientific, R&D, commercial and executive teams
Undertake significant domestic and international travel

Requirements

What you’ll need

Senior leadership experience combining scientific credibility, regulatory expertise, commercial understanding and external leadership skills
Experience in Genome Editing, genetics and genomics, aquaculture, biotechnology, animal breeding, novel technology regulation, market access, government or public affairs, international regulatory strategy, or stakeholder engagement
Relevant education and professional experience in life sciences, biotechnology, genetics, aquaculture, regulatory affairs, public policy, or a related field
Significant regulatory affairs experience within biotechnology, life sciences, animal health, aquaculture, agriculture or another highly regulated science-based industry
Experience developing regulatory strategies for novel or emerging technologies, ideally involving Genome Editing, genetics or genomics
Strong understanding of the pathway from R&D and regulatory strategy through market access to commercial adoption
Ability to engage effectively with regulators, policymakers, industry organizations, clients and other external stakeholders
Scientific and technical depth to engage credibly with scientists, regulators and technical experts
Strong commercial mindset connecting regulatory strategy with market opportunities, client adoption and business priorities
Excellent communication and influencing skills, including translating complex science into clear and credible messages for technical and non-technical audiences
Ability to work across scientific, commercial and executive functions and influence without relying solely on formal authority
Pragmatic, entrepreneurial approach, able to operate strategically while remaining hands-on when required
Strong judgment regarding when to lead internally and when to engage specialist external expertise
Willingness and ability to undertake significant domestic and international travel

Benefits

Comp & perks

Target annual bonus of 20%