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Quality Control Inspector bei None

None · Ronkonkoma, Vereinigte Staaten Von Amerika · Onsite

37.440,00 $  -  41.600,00 $

Jetzt bewerben

Quality Control Inspector 

Job Summary

The 2nd Shift QC Inspector ensures product quality and compliance with FDA regulations and cGMP standards. This role involves performing in-process and final inspections of OTC lip balm, sunscreen, and hand sanitizer, as well as verifying packaging, labeling, and material integrity. The inspector documents findings, reports non-conformances, and works closely with QC, Production, and Warehouse teams to maintain high-quality standards.

Key Responsibilities

  • In-Process Inspections:

    • Perform audits and line checks during production, repacking, and labeling.

    • Verify fill levels, label placement, batch codes, expiration dates, and packaging.

    • Ensure proper line changeovers and adherence to SOPs and GMPs.

  • Finished Product Inspections:

    • Conduct final checks on packaging, labeling, counts, and seal integrity.

    • Approve or reject finished goods before shipment.

  • Documentation & Reporting:

    • Complete inspection records, quality alerts, and batch documentation.

    • Report and escalate deviations or non-conformances promptly.

  • Compliance & Audits:

    • Adhere strictly to current Good Manufacturing Practices (GMPs) and company quality management system (QMS) procedures. 

    • Support internal and external audits as needed.

  • Incoming Material Inspections (as assigned):

    • Inspect raw materials, packaging, and components against specifications.

    • Verify COAs and documentation.

  • Equipment Calibration and Maintenance: 
    • Confirm calibration of inspection tools.

    • Maintain clean, organized inspection areas.

  • Problem Solving and Continuous Improvement: 
    • Assist with investigations and CAPAs.

    • Support quality and process improvement initiatives.

Qualifications

  • Education: High school diploma required; associate’s degree in a technical/scientific field preferred.

  • Experience:

    • 2–3 years in QC within FDA-regulated manufacturing (OTC, cosmetics, or medical devices).

    • Packaging/labeling experience strongly preferred.

  • Skills & Abilities:

    • Strong knowledge of FDA regulations (21 CFR Parts 210, 211, 700–740).

    • Excellent attention to detail and ability to follow SOPs.

    • Strong written and verbal communication skills for documenting findings and interacting with team members. 
    • Basic computer proficiency (Microsoft Office, quality systems).
    • Problem-solving skills; ability to work independently or in a team.

    • Ability to work the designated 2nd shift hours consistently with the potential for start time flexibility from week to week.  

Physical Requirements

  • Ability to stand/walk for extended periods, bend, and lift up to 25 lbs.

  • Good manual dexterity and visual acuity (including color vision) for detailed inspection and sensory tasks. 

  • Comfortable working in varying temperatures, scents, and noise levels.

Work Environment

  • Manufacturing and warehouse setting.

  • Regular exposure to raw materials, packaging components, chemicals, and cleaning agents.


Schedule: Monday through Friday from  12:00pm  - 08:30 PM , and Saturdays from  06:00 AM – 12:00pm 

Pay range: $18.00 – $20.00/hour (depending on experience)


Monday through Friday from 12:00pm - 08:30 PM , and Saturdays from 06:00 AM – 12:00pm
Jetzt bewerben

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