Compliance Officer — Global Supplements & Devices

Every label and every device carries a story of trust — and you’ll be the author of that story. As our Compliance Officer, you won’t just monitor regulations, you’ll shape a system that sets a new global standard for integrity.

You’ll be the calm authority in moments of scrutiny, the voice of clarity in complexity, and the force that transforms compliance into confidence. Each day, you’ll know your work safeguards families, empowers innovation, and builds a legacy of trust across continents.

Here, precision is pride, and every check you complete fuels the freedom for bold ideas to thrive. You’ll reshape the future of how millions experience safe, transparent wellness.

Your next 5 minutes could land you in our top 5% shortlist — click Apply to start your application (a short, simple step to put you in the running) -> https://www.surveymonkey.com/r/Q7YS8L3

ROLE SNAPSHOT —

• Title: Compliance Officer — Global Supplements & Devices
• Location/Schedule: Remote, Full-Time
• Purpose: Build and lead a lean but powerful compliance system for supplements, devices, labeling, and global regulatory execution.

KEY RESPONSIBILITIES —

• Lead supplement compliance: labeling, claims, cGMP, FSMA/FSVP, and packaging requirements.
• Drive device compliance: classification, submissions, labeling, QMS transition, and postmarket reporting.
• Ensure flawless accuracy of all product labeling and claims.
• File all required submissions on time and maintain regulatory records.
• Approve packaging/environmental claims and registrations.
• Build compliance dossiers and lead internal training.

MUST-HAVE QUALIFICATIONS —

• 8–12+ years in dietary supplements and/or medical device compliance.
• Deep expertise in FDA regulations (21 CFR, cGMP, device submissions).
• Strong knowledge of FTC substantiation, Prop 65, COO/import rules.
• Skilled in QMS systems, document control, and label governance.
• Exceptional writing and training ability; thrives in virtual/global teams.

PREFERRED QUALIFICATIONS —

• Direct experience with FDA 483 responses, 510(k) filings, UDI/GUDID, or NDI submissions.
• Success in regulatory inspections without enforcement actions.
• Hands-on SB-343/EPR and Prop 65 compliance.

WHAT WE OFFER —

• The chance to architect compliance systems that set a new global benchmark.
• A lean, focused team where your expertise has direct impact.
• Remote-first culture built on trust, precision, and autonomy.

HONEST CHALLENGE —

Audits will test you, deadlines will press you, and accuracy must be absolute. This role is for leaders who thrive under pressure and take pride in zero-defect execution.

READY TO JUMP IN?

Click Apply to start the short application (about 5 minutes) -> https://www.surveymonkey.com/r/Q7YS8L3