Quality and Regulatory Manager | Los Angeles

TBI Listings Inc.; California; On-site; USD 120,000 - 170,000; Full time

Job summary

Wild & Organic, a US wellness brand in Los Angeles, seeks a Quality & Regulatory Manager to lead quality systems, ensure FDA compliance, and support safe, consistent dietary supplement manufacturing.

You will oversee QMS, document control, supplier qualification, and regulatory submissions, guiding labeling and product changes while mentoring the Quality & Regulatory team.

This on-site role requires a chemistry/biology-related degree and 5–7 years in QA/RA within FDA-regulated settings.

Qualifications

• Bachelor's degree required in relevant field.
• 5–7 years QA/RA experience in FDA-regulated manufacturing.
• 3+ years of leadership experience.

Responsibilities

• Lead and maintain QMS and SOPs.
• Ensure compliance with FDA, cGMP, GDP.
• Oversee document control, CAPA, change control, deviations.
• Review and approve MMRs, BPRs, specifications, SOPs.
• Lead investigations (deviations, complaints, OOS/OOT).
• Manage internal audits and represent the company during FDA inspections.
• Oversee supplier qualification and validation programs.
• Provide regulatory guidance for labeling, ingredients, and new products.
• Lead and develop Quality & Regulatory team members.

Skills

QA/RA experience

Leadership

FDA inspections

GMP audits

CAPA

Change control

Deviation management

Validation programs

Supplier qualification

21 CFR Part 111

cGMP

GDP

Analytical skills

Communication

Education

Bachelor's degree in Chemistry, Biology, Food Science, Microbiology, QA/RA or related field

Job description

# Quality and Regulatory Manager | Los Angeles## Northridge, California (On‐Site) Full‐Time Brand: Wild & Organic Industry: Dietary Supplements (FDA 21 CFR Part 111 & 117) About Us Wild & Organic is a US wellness brand producing high‐quality dietary supplements. We're looking for a Quality & Regulatory Manager to lead our quality systems, ensure FDA compliance, and support safe, consistent manufacturing operations. Requirements — Bachelor's degree in Chemistry, Biology, Food Science, Microbiology, QA/RA or related field — 5–7 years of QA/RA experience in FDA‐regulated manufacturing — 3+ years of leadership experience — Strong knowledge of 21 CFR Part 111, cGMP, GDP — Experience with FDA inspections, GMP audits, CAPA, Change Control, Deviation Management — Experience with validation programs & supplier qualification — Strong analytical and communication skills Key Responsibilities — Lead and maintain QMS & SOPs — Ensure compliance with FDA, cGMP, GDP — Oversee document control, CAPA, change control, deviations — Review and approve MMRs, BPRs, specifications, SOPs — Lead investigations (deviations, complaints, OOS/OOT) — Manage internal audits and represent the company during FDA inspections — Oversee supplier qualification and validation programs — Provide regulatory guidance for labeling, ingredients, and new products — Lead and develop Quality & Regulatory team members