Senior Quality & Regulatory Lead – Dietary Supplements (FDA)

TBI Listings Inc.

California

Presencial

USD 120.000 - 170.000

Jornada completa

14 días+

Una candidatura completa en un minuto

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Descripción de la vacante

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.

Formación

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

Responsabilidades

  • 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.

Conocimientos

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

Educación

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

Descripción del empleo

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.

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