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Internship Quality Manager Jobs (NOW HIRING)

FOOD FUSION NJ LLC

Quality Inspector

Bridgeton, NJ · On-site

$18 - $21/hr

... Manager / Quality Director FLSA Status | Non-Exempt Work Schedule | Production shift schedule ... related field (internship or co-op experience counts) * Basic understanding of food safety ...

FOOD FUSION NJ LLC

Quality Inspector

Bridgeton, NJ · On-site

$18 - $21/hr

... Manager / Quality Director FLSA Status | Non-Exempt Work Schedule | Production shift schedule ... related field (internship or co-op experience counts) * Basic understanding of food safety ...

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Infographic showing various Internship Quality Manager job openings in the United States as of July 2026, with employment types broken down into 9% Internship, 1% As Needed, 68% Full Time, 20% Part Time, 1% Temporary, and 1% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution.

Quality Inspector

FOOD FUSION NJ LLC

Bridgeton, NJ • On-site

$18 - $21/hr

Full-time

Re-posted 7 days ago

Job description

Quality Technician

Food Manufacturing | Entry-Level | Full-Time
Department | Quality Assurance
Reports To | Quality Manager / Quality Director
FLSA Status | Non-Exempt
Work Schedule | Production shift schedule; overtime and weekend availability may be required
Regulatory Scope | FDA/FSMA (21 CFR Part 117), USDA/FSIS (9 CFR Part 417, 416), SQF Code

Position Summary

The Quality Technician supports the quality assurance function by performing in-process inspections on the production floor, maintaining accurate regulatory and SQF documentation, and conducting receiving inspections on incoming raw materials and ingredients. This is an entry-level role designed for candidates who are detail-oriented, comfortable working in a fast-paced manufacturing environment, and eager to develop expertise in food safety compliance.

Key Responsibilities

Production Floor Quality Control


  • Perform scheduled in-process checks including weight, temperature, pH, water activity (aw), visual appearance, and packaging integrity

  • Monitor Critical Control Points (CCPs) and verify that critical limits are met per the facility HACCP plan (9 CFR 417 / 21 CFR 117)

  • Observe and document pre-operational and operational sanitation checks in accordance with Sanitation SOPs (9 CFR 416)

  • Identify, tag, and initiate holds on nonconforming product; communicate immediately to the Quality Manager

  • Support environmental monitoring swab collection and sample submission per the facility EMP schedule

  • Verify that allergen changeover and line clearance procedures are completed and documented before production begins

Documentation & Compliance


  • Complete all required production and quality records accurately and in real time; never pre-fill or back-fill records

  • Maintain records in compliance with FSIS record retention requirements (9 CFR 412) and FDA 21 CFR 117 recordkeeping requirements (minimum 2 years for most records)

  • Assist in label verification: confirm product label matches approved artwork, including allergen declarations (FALCPA Big 9), net weight, and lot coding

  • Support internal SQF audits and FDA/USDA inspection readiness by organizing records and ensuring documentation is complete and legible

  • Participate in corrective action and preventive action (CAPA) documentation; assist in root cause analysis under direction of Quality Manager

  • Log nonconformances and assist with drafting responses to FSIS Noncompliance Records (NRs) when applicable

Supplier & Incoming Quality


  • Conduct receiving inspections on raw materials, ingredients, and packaging; verify supplier COAs against approved specifications

  • Review and file Certificates of Analysis (COAs), temperature records, and shipping documents for incoming lots

  • Reject or place on hold any incoming material that does not meet specifications; document and notify Purchasing and Quality Manager

  • Assist in maintaining the approved supplier list and supplier verification records per FSMA supply-chain program requirements (21 CFR 117 Subpart G)

  • Support foreign supplier verification activities (FSVP) as directed, including reviewing importer documentation under 21 CFR Part 1 Subpart L

Qualifications

Required


  • High school diploma or GED; 

  • 0–2 years of experience in food manufacturing, quality control, or a related field (internship or co-op experience counts)

  • Basic understanding of food safety principles, GMP, and HACCP concepts

  • Ability to read, write, and communicate clearly in English; bilingual (English/Spanish) a plus

  • Comfortable working in cold, wet, or hot production environments; ability to stand for extended periods

  • Strong attention to detail and commitment to accurate recordkeeping

Preferred


  • Familiarity with SQF, BRC, or other GFSI-recognized food safety schemes

  • Experience using electronic quality management systems (QMS) or ERP platforms

  • PCQI certification (FDA Preventive Controls Qualified Individual) or willingness to obtain

  • Basic lab skills: pH meter, water activity meter, moisture balance

Work Environment & Physical Requirements

This position requires work in an active food manufacturing environment. Conditions include exposure to noise, temperature variation (refrigerated and ambient areas), wet floors, and food processing equipment. Employees must comply with all GMP requirements including hair nets, beard nets, gloves, and appropriate PPE at all times on the production floor.


Physical demands include: standing for up to 8–12 hours per shift, lifting up to 40 lbs, bending, reaching, and walking production lines. Reasonable accommodations may be made for individuals with disabilities.