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Product Quality Coordinator

Job in Leonia, Bergen County, New Jersey, 07605, USA
Listing for: Experis Technology Group
Full Time position
Listed on 2026-09-28
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, Regulatory Compliance Specialist, QA Specialist - Analyst/Manager, Quality Engineering
Salary/Wage Range or Industry Benchmark: 20 - 28 USD Hourly USD 20.00 28.00 HOUR
Job Description & How to Apply Below

Our client, a leading organization in the food and beverage industry, is seeking a Coordinator Product Quality to join their team. As a Coordinator Product Quality, you will be part of the Quality Laboratory supporting laboratory services to ensure product safety, regulatory compliance, and customer satisfaction. The ideal candidate will demonstrate attention to detail, proactive communication skills, and a commitment to quality standards, which will align successfully in the organization.

Job Title:
Product Quality Coordinator

Location:
Leonia, NJ

Pay Range: $24/hr
Must Have:

  • Sample management and sample tracking (raw materials, bulk products, lab submissions)
  • GMP/GDPknowledge
  • Experience working in a laboratory, manufacturing, Food & Beverage, pharma, Nutraceuticals, Consumer Products,Cosmetics,Chemical Manufacturingor regulated environment

What's the Job?

  • Support the Quality Laboratory mission by managing routine sample submissions and testing coordination.
  • Communicate effectively with internal teams and external stakeholders regarding sample status and documentation issues.
  • Maintain accurate reports, logs, and data trending related to quality testing processes.
  • Review certificates of analysis, QA/QC reports, and other quality documentation for raw materials and products.
  • Assist during annual audits and support laboratory operations, including procurement and invoice management.

What's Needed?

  • Proficiency in Microsoft Office and basic mathematical and analytical skills.
  • Ability to read and understand chemistry, microbiology terminology, and documentation.
  • Familiarity with GMP, Good Documentation Practices, ISO 17025, SHE principles, and Nestlé QMS.
  • Strong verbal and written communication skills in English.
  • Ability to work collaboratively within teams and adapt to changing work environments.

What's in it for me?

  • Opportunity to contribute to product safety and quality assurance in a reputable organization.
  • Engagement in a dynamic work environment with a focus on continuous improvement.
  • Development of skills in laboratory operations and quality management systems.
  • Participation in a supportive and inclusive workplace culture.
  • Potential for career growth within the organization.

Upon completion of waiting period consultants are eligible for:

  • Medical and Prescription Drug Plans
  • Dental Plan
  • Vision Plan
  • Health Savings Account
  • Health Flexible Spending Account
  • Dependent Care Flexible Spending Account
  • Supplemental Life Insurance
  • Short Term and Long Term Disability Insurance
  • Business Travel Insurance
  • 401(k), Plus Match
  • Weekly Pay
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