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QA Associate

Job in Morristown, Morris County, New Jersey, 07960, USA
Listing for: System One
Full Time position
Listed on 2026-02-16
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control / Manager, Quality Technician/ Inspector, QA Specialist / Manager
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Job Title
: QA Associate
Location
:
Florham Park area (Hybrid)
Hours / Schedule
: 9am - 5pm
Type
:
Direct Hire

The QA 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.
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.
Benefits
  • Health, Dental, and Vision coverage starting Day 1.
  • 401(k) with employee contributions.
  • Profit‑sharing eligibility after 6 months.

#M3
: #558-Scientific

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Position Requirements
10+ Years work experience
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