Senior Global Product Compliance Specialist
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 2d ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
Posted 14d ago
The date the source published, not the day we noticed it (2026-10-20). Last seen at its source 7h ago.
We have tracked this listing since 20 Oct 2026 (13 days). The employer's own board has carried it every time we have read it, most recently 7 hours ago.
Is it remote?
Marked remote on the employer's board
Their board carries a remote setting on this posting — a field they filled in, not wording we read. The location field names somewhere specific, which is usually where the team or the entity sits.
Who may apply?
United States
The description states no restriction of its own. This is the source's own tag.
Pay not stated
Similar roles pay $170k–222.4k/yr
Middle 50% of 426 listings that do state pay — Product · Senior · United States · USD/year. This employer has published no salary; this is what comparable listings we hold disclose, never converted between currencies or periods. How this is calculated.
Skills named in the ad
Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.
Carried by 1 source
-
Workable employer's own board first seen 13d ago · last seen 7h ago
The listing
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.
Our mission is simple: help billions of people live healthier lives for longer, and ultimately, Don’t Die.
The Sr. Global Product Compliance Specialist is a full-time, expert-level individual contributor reporting to the VP, Global Product Compliance. This role independently manages market-specific compliance projects supporting Blueprint product development, launch, and ongoing commercialization in the U.S. and international markets, including the EU, APAC, Middle East, North America, and Australia. The portfolio includes dietary supplements, conventional foods, cosmetics, and medical devices, with potential support for OTC drugs as the portfolio evolves. There are no direct reports initially; infrequent travel is required.
Requirements
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.
Benefits
Salary Range: $135-180k + equity + benefits