Quality Control Inspector bei None
None · Ronkonkoma, Vereinigte Staaten Von Amerika · Onsite
- Professional
- Optionales Büro in Ronkonkoma
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