Quality Auditor - Lebanon

Posted Yesterday
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Lebanon, PA, USA
In-Office
Senior level
Logistics • Professional Services • 3PL: Third Party Logistics • Manufacturing
The Role
Perform production-line quality inspections and audits to ensure FDA and cGMP compliance; conduct AQL checks; record lot/date/label data; quarantine nonconforming materials; monitor batch records and validation protocols; collaborate with Production and Quality Management to resolve issues.
Summary Generated by Built In

Quality Auditor

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!

Skills Required

  • 5+ years of GMP/QA experience in a manufacturing environment (or equivalent relevant experience).
  • Strong knowledge of FDA and cGMP regulations.
  • Experience performing inspections, audits, and Acceptance Quality Limits (AQL) checks.
  • Confirming and recording date codes, lot numbers, expiration dates, and labeling accuracy.
  • Place non-conforming materials in quarantine and document deviations; monitor batch records and validation protocols.
  • Excellent communication, problem-solving, and teamwork skills.
  • Ability to work independently, manage multiple tasks, and adapt to changing priorities.
  • High School Diploma or GED.
  • Bilingual (a plus).
  • 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.
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The Company
450 Employees
Year Founded: 2008

What We Do

Synergies Companies is an umbrella brand providing end-to-end solutions for staffing, packaging, fulfillment, and distribution. The company operates through three specialized divisions: Staffing Synergies, which provides light industrial staffing for manufacturing and warehouses; Synasha, offering contract manufacturing and packaging; and Diversified Synergies, focusing on kitting and fulfillment for pharmaceutical, food and beverage, and consumer goods clients.

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