Quality Auditor - Edison

Staffing-Synergies; Edison (NJ); On-site; USD 70,000 - 100,000; Full time

Job summary

Staffing Synergies seeks a detail-oriented Quality Auditor to join our team. You’ll ensure that products meet FDA, cGMP, and customer requirements, perform inspections on production lines, and help drive quality across operations.

The role requires 5+ years of GMP/QA experience, strong knowledge of FDA regulations, and excellent communication and teamwork. A High School Diploma or GED is required, with ability to stand for long periods and lift up to 25 lbs.

Qualifications

• 5+ years of GMP/QA experience in a manufacturing environment.
• Strong knowledge of FDA and cGMP regulations.
• Excellent communication, problem-solving, and teamwork skills.

Responsibilities

• 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.

Skills

QA Experience

GMP Knowledge

FDA Regulations

Communication Skills

Teamwork

Education

High School Diploma or GED

Job description

Career Opportunities with Staffing Synergies

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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.

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