International Regulatory Compliance Manager

Confirmed live in the last 24 hours

Dr. Squatch (men's natural grooming/wellness)

Compensation

$100,000 - $120,000/year

Marina del Rey, California, United States

Hybrid

Posted April 3, 2026

Job Description

Why We Exist and What We Do:

At Dr. Squatch (www.drsquatch.com), we’re raising the bar on men’s personal care with our line of natural, high-performance products. We’re on a high-growth, fast-moving ride, continually introducing new product categories, launching into retailers nationwide, and growing internationally. We have been recognized and certified by Great Place to Work® multiple times, and we achieved status as a certified B Corp in 2023. We are looking for passionate, talented people who want to join us in our mission to inspire and educate men to be happier and healthier!

About the Role:

Dr. Squatch is seeking an International Regulatory Compliance Manager responsible for enabling Dr. Squatch’s global growth by ensuring products are compliant and market-ready across key regions including Canada, UK, EMEA, LATAM, Australia, and future markets.

This role owns end-to-end regulatory execution, from product registrations and documentation to claims and labeling compliance, while serving as the primary point of contact for EU/UK and Canada Responsible Persons. Working cross-functionally, this individual will embed regulatory requirements into product development and launch processes, ensuring efficient and compliant market access.

This is a hands-on role in a fast-paced environment, requiring strong ownership, collaboration, and the ability to translate complex regulations into clear, actionable guidance.

This role will report to the Sr. Compliance Manager.

This is a full-time, hybrid role with company benefits based in Marina del Rey, CA.

The anticipated base compensation range for this role will be $100,000 to $120,000. Compensation will be commensurate with the candidate's experience and local market rates.

What You'll Do:

Own regulatory compliance and market access across global markets, including Canada, UK, EMEA, LATAM, Australia, and future expansion regions
Serve as the primary point of contact for EU/UK and Canada Responsible Persons (RPs)
Develop and execute regulatory strategies to support international product launches and expansion
Translate evolving regulatory requirements into clear, actionable guidance for internal teams
Lead preparation and submission of global product notifications and registrations (e.g., CPNP, SCPN, Health Canada CNF, AICIS, etc.)
Ensure all products meet local regulatory requirements prior to market entry
Manage post-market obligations, renewals, and ongoing compliance activities
Prepare, review, and maintain Product Information Files (PIFs) and equivalent dossiers, ensuring they are complete, accurate, and audit-ready
Gather, assess, and validate supplier technical documentation (e.g., COAs, SDS, specifications)
Ensure all safety and technical documentation aligns with regulatory requirements
Review and substantiate product claims in partnership with internal stakeholders
Review and approve artwork, labeling, and marketing materials for regulatory compliance
Embed regulatory checkpoints into product development and artwork workflows
Partner closely with Product Development, Commercialization, Marketing, Supply Chain, and Quality teams to support compliant product innovation and launches
Represent Regulatory on project teams, providing guidance on timelines, risks, and requirements
Enable efficient and compliant product lifecycle management
Manage and oversee external regulatory consultants, Responsible Persons, and distributors
Ensure timely and accurate completion of global registrations while maintaining internal accountability
Build strong relationships with regulatory partners