Senior Global Product Compliance Specialist

About the role

Death is our only foe.

Immortals was founded by Bryan Johnson and Kate Tolo to build a new standard for human health and longevity.

We’re building Autonomous Health: a system that uses measurement, scientific evidence, and personalization to help people understand their bodies and make better decisions about their health. What began with Bryan becoming the most measured person in history is becoming a platform for everyone.

Immortals brings together biomarkers, longevity medicine, nutrition, prescriptions, wearables, and personalized protocols in one place, turning health data into clear, actionable decisions.

We’re a small, ambitious team building what we believe will become the new operating system for human health. We move quickly, think from first principles, care deeply about the quality of our work, and hold ourselves to an unusually high standard.

Position Responsibilities

• Manage domestic and international compliance projects from feasibility through launch and ongoing maintenance; establish regulatory pathways, requirements, deliverables, and timelines with cross-functional teams.
• Evaluate ingredient sources, permitted uses, daily intake limits, formulation suitability, and product classification; recommend compliant formulations and market-specific adaptations.
• Prepare and manage product registrations, notifications, licenses, renewals, and change submissions; coordinate supporting documentation, authority responses, external consultants, distributors, and other market partners.
• Review and approve routine labels, packaging, localized translations, claims, advertising, and product-related website content within delegated authority; evaluate supporting substantiation and recommend compliant language.
• Monitor regulatory developments, assess business impact, maintain regulatory records and procedures, and communicate practical guidance to Product Development, Marketing, Operations, Supply Chain, Quality, and Legal.
• Independently resolve routine regulatory issues and escalate significant risks, unresolved interpretations, exceptions, and material business decisions to the VP, Global Product Compliance. Quality retains ownership of supplier qualification, specifications/COA approval, GMP compliance, complaints, adverse events, and recalls.

Basic Qualifications

• Demonstrated dietary supplement regulatory affairs or product compliance experience, including independent formula, label, and claims assessments.
• Ability to research and interpret regulations, scientific literature, formulas, and technical documentation and translate findings into practical recommendations.
• Strong project management skills, including managing competing priorities, regulatory submissions, timelines, and external partner deliverables.
• Strong analytical judgment, technical writing, and communication skills, including documenting regulatory decisions and escalating significant risks.
• Ability to work independently in a fully remote environment and collaborate effectively with cross-functional teams, consultants, and market partners.
• Proficiency with Microsoft Word, Excel, PowerPoint, and shared project and document management tools.

Preferred Skills

• Bachelor’s degree in a relevant scientific or technical discipline.
• 5–7 years of relevant regulatory affairs or product compliance experience.
• International dietary supplement experience, particularly across the EU, APAC, Middle East, North America, and Australia.
• Experience managing international product registrations, market-entry assessments, localized labeling, and regulatory consultants.
• Additional regulatory experience with conventional foods, cosmetics, medical devices, or OTC drugs.