Quality Auditor - Edison

Staffing Synergies

  • Edison, NJ
  • 27 days ago
  • $18 Per Hour
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Skills

  • Auditingunmatched
  • Communication Skillsunmatched
  • Current Good Manufacturing Practice (cGMP)unmatched
  • Detail Orientedunmatched
  • Documentationunmatched
  • FDA (Food and Drug Administration)unmatched
  • FDA Requirementsunmatched
  • GMP (Good Manufacturing Practices)unmatched
  • High School Diplomaunmatched
  • Lift/Move 25 Poundsunmatched
  • Maintain Complianceunmatched
  • Manufacturingunmatched
  • Multilingualunmatched
  • Multitaskingunmatched
  • Problem Solving Skillsunmatched
  • Quality Assuranceunmatched
  • Quality Controlunmatched
  • Quality Managementunmatched
  • Safety Complianceunmatched
  • Safety Standardsunmatched
  • Standard Operating Procedures (SOP)unmatched
  • Team Playerunmatched
  • Validation Planunmatched

Description

Quality Auditor

Location: Edison, NJ

Pay: $18/hr

Shift:

1st shift - 6:00am-2:45pm

2nd shift - 3:00pm-11:45pm

Join Our Team at Staffing Synergies!
We are looking for a detail-oriented Quality Auditor to join our team. In this role, you’ll play a key part in ensuring that our products meet the highest standards of quality, safety, and compliance. If you thrive in a fast-paced environment and take pride in precision, this is the opportunity for you!

What You’ll Do:

  • Perform quality inspections on production lines to ensure compliance with FDA, cGMP, SOPs, and customer requirements.
  • Partner with Production and Quality Management to resolve quality issues in real time.
  • Conduct inspections, audits, and Acceptance Quality Limits (AQL) checks to verify product integrity.
  • Confirm and record date codes, lot numbers, expiration dates, and labeling accuracy.
  • Place non-conforming materials in quarantine and document all deviations.
  • Monitor batch records, validation protocols, and ensure proper documentation is completed.

What We’re Looking For:

  • 5+ years of GMP/QA experience in a manufacturing environment (or equivalent relevant experience).
  • Strong knowledge of FDA and cGMP regulations.
  • Excellent communication, problem-solving, and teamwork skills.
  • Ability to work independently, manage multiple tasks, and adapt to changing priorities.
  • High School Diploma or GED required.
  • Bilingual a plus!

Physical Requirements:

  • Ability to stand for long periods (8+ hours).
  • Able to lift up to 25 lbs occasionally.
  • Comfortable with bending, squatting, reaching, and repetitive hand/finger use.

If you’re passionate about quality and want to make an impact, apply today!

Numbers & Facts

LocationEdison, NJ

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