Regulatory Affairs Specialist (remote)

California, California Permanent USD60,000 - USD80,000 per year View Job Description
We are seeking an experienced Regulatory Affairs Specialist to support compliance and regulatory processes in the Quality department. This role is remote.
  • Growing Manufacturer
  • Growth Opportunity

About Our Client

Our client is a well-established, mid-sized company operating in the supplements/OTC industry.

Job Description

  • Experince working with Supplements or OTC is required.
  • Experience with FDA regulatory frameworks, including 21 CFR Parts 111, 101, and 330, with the ability to interpret and apply regulations to OTC drug monographs and dietary supplement requirements.
  • Strong Labeling Compliance expertise, including review of Supplement Facts / Drug Facts panels, ingredient statements, allergen labeling, claims language, and packaging artwork to ensure alignment with FDA, FTC, and cGMP requirements.
  • Hands‑on experience conducting claims substantiation, reviewing scientific literature, and ensuring all structure/function and OTC‑permitted claims are properly supported and risk‑appropriate.
  • Ability to review and assess raw materials, including COAs, SDSs, specifications, and vendor documentation for regulatory acceptability and compliance with internal quality standards.
  • Familiarity with product development workflows, including evaluating ingredient permissibility, tracking formulation changes, advising on regulatory risks, and supporting cross‑functional teams (R&D, Quality, Marketing, Legal).
  • Knowledge of international regulatory requirements (preferred but not required), including Canada NNHP, EU/UK supplement standards, and global OTC compliance frameworks.

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants. Michael Page will consider for employment qualified applicants with criminal histories in a manner consistent with the Los Angeles Fair Chance Initiative for Hiring Ordinance.

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.

The Successful Applicant

A successful Regulatory Affairs Specialist should have:

  • Knowledge of regulatory standards and requirements in the Engineering & Manufacturing sector.
  • Strong organizational skills and attention to detail for managing documentation.
  • Excellent communication abilities to liaise with internal teams and external regulatory bodies.
  • Problem-solving skills to navigate complex regulatory challenges.
  • Familiarity with compliance audits and inspections.

What's on Offer

  • Competitive annual salary ranging from $60,000 to $80,000 USD.
  • Comprehensive benefits package including 401(k).
  • Opportunity to work in a thriving and innovative industry.
  • Be part of a collaborative and supportive work environment.



If you're ready to take the next step in your career as a Regulatory Affairs Specialist in Los Angeles, we encourage you to apply today!

Contact
Rishab Vaidhyanathan
Quote job ref
JN-032026-6984592

Job summary

Sector
Engineering & Manufacturing
Sub Sector
Quality, Technical
Industry
Healthcare / Pharmaceutical
Location
California
Contract Type
Permanent
Consultant name
Rishab Vaidhyanathan
Job Reference
JN-032026-6984592