Director, International Product Compliance

Blueprint

5h•$175 - $225

About The Position

Death is our only foe. Blueprint was founded by Bryan Johnson, who has the world’s best comprehensive biomarkers. He is quantitatively the healthiest person on the planet. Blueprint is methodically built on science. Bryan freely shares his protocol, learnings and data with everyone to use. Blueprint has also developed a family of nutritional products to make the benefits of the Blueprint protocol affordable and available to all. We’re a small, tight-knit team working to clean up the global food supply, provide healthy food to everyone, and build Don’t Die into the most influential ideology in the world. We move quickly, work efficiently, and enjoy an environment defined by competence. With strong continuing success in the US under our belt, we're now looking at international market expansion. To support this expansion, we're looking for a Director, International Product Compliance to own global regulatory strategy across international and U.S. markets, with emphasis on international market entry and scalable oversight of U.S. regulatory activities. The successful candidate would spearhead coordination with regulatory consultants and our R&D, operations, legal, finance and commercial teams to develop and execute rapid market entry strategies globally.

Requirements

8–12+ years of regulatory affairs / international compliance experience in:
Dietary supplements, nutraceuticals, functional foods, or other regulated consumer health products
Proven experience managing registrations across multiple global markets
Strong understanding in one or more, and ability to source information on others:
FDA & cGMPs
EFSA / EU Novel Foods
Health Canada NHP
CFDA / NMPA (China)
TGA (Australia), FSANZ
Other ASEAN and LATAM frameworks
Demonstrated experience with claims substantiation, ingredient approvals, and labeling compliance
Strong command of:
International product registration workflows
Import/export regulatory requirements
Customs and trade compliance
Regulatory documentation systems
Comfortable interfacing with:
Laboratories, notified bodies, consultants, distributors, and government authorities
Experience building scalable regulatory processes in growth-stage or multinational organizations
Strategic, commercially minded regulatory leader — not just tactical
Able to balance speed-to-market with regulatory rigor
Excellent fast communicator capable of translating regulations into actionable business guidance
Highly organized, detail-oriented, and capable of managing parallel global projects
Comfortable working cross-culturally and across time zones
Bachelor’s degree required (Life Sciences, Regulatory Affairs, Food Science, Chemistry, or related field preferred)

Nice To Haves

Advanced degree or regulatory certifications (e.g., RAC) a plus

Responsibilities

Own the global regulatory roadmap supporting international expansion across key regions (e.g., EU, UK, Canada, China, Japan, Korea, ASEAN, LATAM, Middle East)
Assess regulatory feasibility for new markets, products, and formulations
Develop market entry strategies balancing speed-to-market with compliance and risk
Lead preparation, submission, and maintenance of product registrations, notifications, and approvals globally, with the assistance of consultants as necessary
Oversee technical dossiers, ingredient approvals, and formula assessments per jurisdiction
Manage post-approval lifecycle including renewals, variations, and amendments
Ensure compliance with country-specific import requirements including labeling, claims, customs documentation, tariffs, and certificates
Partner with Supply Chain and Logistics on cross-border compliance, HS codes, COO, COAs, and trade documentation
Support distributor and customs authority interactions where necessary
Monitor evolving global regulatory landscapes affecting dietary supplements, functional foods, nutraceuticals, cosmetics and devices.
Anticipate regulatory changes and proactively adjust strategy
Identify and mitigate regulatory, compliance, and product liability risks
Serve as a strategic advisor to Product Development on globally viable formulations and claims
Collaborate with Quality and Manufacturing on compliance with GMP, audits, required certifications and regulatory inspections
Train internal stakeholders on regulatory requirements and best practices
Act as primary Blueprint representative with global regulatory authorities and external consultants
Build relationships with international regulators, trade associations, and testing bodies
Manage third-party regulatory service providers efficiently and cost-effectively
Build and maintain regulatory SOPs, templates, and internal compliance systems
Ensure documentation supports audits, inspections, and due diligence (including support for M&A or investor reviews)