Quality Control Inspector

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)