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QC Inspector 3rd Shift

Job in Wharton, Morris County, New Jersey, 07885, USA
Listing for: Zing Recruiting
Full Time position
Listed on 2026-07-15
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, Production QC/QA
Salary/Wage Range or Industry Benchmark: 22 - 23 USD Hourly USD 22.00 23.00 HOUR
Job Description & How to Apply Below

Position Title

Quality Control Line Inspector

Department

Quality Control

Reports To

QC Supervisor / QC Manager / Director of Quality Control

Position Summary

The Quality Control (QC) Line Inspector is responsible for performing in-process inspections on manufacturing and packaging lines to ensure that cosmetic and OTC drug products are produced in compliance with current Good Manufacturing Practices (cGMP), internal quality standards, and regulatory requirements, including 21 CFR Parts 210 and 211.

Key Responsibilities
  • In-Process Line Inspection
    • Perform routine inspections of filling, labeling, and packaging lines
    • Verify line clearance prior to start-up
    • Inspect fill levels, container integrity, labeling accuracy, and coding
    • Identify and report defects such as leaks, mislabels, or contamination
  • Compliance & Documentation
    • Ensure adherence to cGMP (21 CFR 210/211) and SOPs
    • Complete inspection logs, batch records, and deviation reports
    • Escalate non-conformances and support investigations
  • Line Clearance & Setup Verification
    • Conduct line clearance during changeovers
    • Verify correct components (labels, cartons, containers)
    • Confirm reconciliation of materials
  • Sampling & Testing
    • Collect in-process samples per sampling plans
    • Perform visual and basic inspection checks
    • Submit samples to QC lab when required
  • Batch Record Support
    • Ensure documentation meets GDP (ALCOA+) standards
    • Identify discrepancies during production
  • Collaboration
    • Work cross-functionally with Production, QA, and Warehouse
    • Support audits (internal, customer, FDA)
Qualifications
  • Education
    • High school diploma or GED required
    • Associate degree preferred
  • Experience
    • 1–3 years in cosmetic or OTC manufacturing
    • Experience in FDA-regulated environments preferred
  • Technical Knowledge
    • Familiarity with 21 CFR Parts 210 & 211
    • Understanding of cGMP and documentation practices
  • Skills
    • Strong attention to detail
    • Effective communication and escalation
    • Basic math and inspection skills
    • Ability to work in a fast-paced environment
Physical Requirements
  • Prolonged standing
  • Visual inspection capability
  • Ability to lift up to 25–50 lbs
Work Environment
  • Manufacturing floor with PPE requirements
  • May require shift work, weekends, or overtime
Key Performance Indicators
  • Pay Rate: $22.00 to $23.00 per hour
  • Reduction in defects and deviations
  • Documentation accuracy
  • Audit readiness and compliance
Equal Opportunity Employer

ZING is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive workplace for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other status protected by applicable law.

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