QA Associate

7 days ago

Morristown NJ, United States Joulé Full time

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. Make sure to read the full description below, and please apply immediately if you are confident you meet all the requirements. 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. xrczosw 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

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