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Quality Assurance Supervisor

Job in Erlanger, Kenton County, Kentucky, 41018, USA
Listing for: Randstad USA
Full Time, Part Time position
Listed on 2026-07-15
Job specializations:
  • Quality Assurance - QA/QC
    QA Specialist - Analyst/Manager, Regulatory Compliance Specialist, Quality Control - QC Analysts/Managers, Production QC/QA
Salary/Wage Range or Industry Benchmark: 65000 - 90000 USD Yearly USD 65000.00 90000.00 YEAR
Job Description & How to Apply Below

Overview

We are seeking a high‑caliber, hands‑on Quality Assurance Supervisor to lead day‑to‑day quality compliance and operational oversight at our FDA‑registered API distribution facility in Kentucky. In this critical, on‑site role, you will lead a dedicated QA Specialist within a close‑knit, highly collaborative team of three, serving as the primary quality presence on the warehouse floor to ensure all receiving, storage, temperature control, mapping, and distribution activities strictly align with FDA cGMP (21 CFR Parts 210/211), GDP, and ICH Q7 guidelines.

The ideal candidate brings 6–10 years of pharmaceutical QA experience (including 3+ years in a pharmaceutical warehouse, distribution, or 3PL environment), proven supervisory experience, and expert‑level competency in authoring deviations, root cause analysis, and CAPA management.

Most importantly, you will serve as the primary quality management representative during high‑stakes corporate, customer, and FDA inspections, ensuring the facility remains in a constant state of total inspection readiness.

This full‑time, Monday‑Friday (8:00 AM – 5:00 PM) position requires 40–50 hours per week depending on operational needs, offers competitive pay up to $90,000 per year, and features an expedited, multi‑round virtual and on‑site interview process for an immediate hire.

Responsibilities
  • Lead quality compliance and operational oversight for receiving, storage, temperature control, mapping, and distribution activities.
  • Supervise a QA Specialist and serve as primary quality presence on the warehouse floor.
  • Author deviations, conduct root cause analysis, and manage CAPA activities.
  • Represent the facility during corporate, customer, and FDA inspections to maintain inspection readiness.
Skills and Experience
  • FDA (minimum 2 years of experience)
  • Quality Control (minimum 2 years of experience)
  • Quality Assurance (minimum 6 years of experience)
  • Audits (minimum 6 years of experience)
  • Pharmaceutical (minimum 6 years of experience)
  • Supervisor (minimum 6 years of experience)
Qualifications
  • Minimum 6 years of experience in pharmaceutical QA.
  • Experience level:
    Experienced.
Experience & Education
  • Experience:

    Experienced, 6 years.
  • Education:

    Bachelor’s degree (required).
Compensation

Salary: $65,000 – $90,000 per year.

Shift: First.

Working hours:

8 AM – 4 PM. Position:
Full‑time, Monday to Friday. 40–50 hours weekly depending on operational needs.

Benefits

The company offers a comprehensive benefits package, including medical, prescription, dental, vision, AD&D, life insurance, short‑term disability, and 401(k) plan (subject to eligibility).

Equal Opportunity Employment

Equal Opportunity

Employer:

Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Accommodations

Applicants requiring reasonable accommodation to make the application or interview process accessible can contact

Additional Information

The posting is open for thirty (30) days.

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