QA Associate

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  • Consulting
  • FullTime
  • Applications have closed

Job Title: Quality Assurance Associate

Location: Morristown, New Jersey (Hybrid)

Type: Direct Hire

Hours: 9am-5pm

Requirements:

  • 1–3 years of Quality Assurance experience in the food, dietary supplement, or nutraceutical industry.
  • Knowledge of FDA food regulations, HACCP, and HARPC
  • Strong skills in managing technical and controlled documentation.
  • Excellent communication skills, including handling client-facing QA documentation.
  • Proficiency in Microsoft Office and ability to learn new systems like Compliance Quest or Salesforce.
  • Understanding of food or ingredient specifications, including assays, contaminants, allergens, GMOs, and flow charts
  • Ability to interpret Certificates of Analysis (CoAs) and regulatory documents
  • Familiarity with FDA guidelines and industry standards for testing and compliance
  • Knowledge of supplier and product approval processes
  • Strong communication skills across departments (Sales, QA, Regulatory, Customer Service)
  • Ability to explain technical issues to both technical and non-technical audiences
  • Skilled at coordinating and engaging with internal and external stakeholders
  • Align customer needs with internal quality standards
  • Balance customer satisfaction with regulatory and safety compliance
  • Manage risk in product testing, supplier validation, and release decisions
  • Knowledge of internal release procedures and documentation standards
  • Ability to follow or develop fast-track processes while maintaining compliance

The Quality Assurance Associate will support quality and regulatory functions by coordinating technical documentation and managing sampling activities (non-lab). This associate-level role is ideal for individuals with 1–3 years of QA experience in the food, dietary ingredient, or nutraceutical industry. The successful candidate will be detail-oriented, comfortable working across teams, and interested in contributing to high-quality compliance processes.

Responsibilities:

  • Coordinate and manage Controlled Documents (CDs) and other technical documentation.
  • Handle non-lab product sampling, including coordination, receipt, storage, and dispatch with required paperwork.
  • Assist in maintaining and uploading QA documentation in the Compliance Quest system.
  • Respond to client and internal inquiries regarding product and facility documentation.
  • Cross-check specifications for alignment with customer requirements.
  • Support broader QA initiatives and projects as directed by the Associate Director, Quality.

BENEFITS

  • Health, Dental, and Vision coverage starting Day 1
  • 401(k) with employee contributions
  • Profit-sharing eligibility after 6 months