Quality Auditor
Staffing Synergies•Edison, NJ
•Onsite
About The Position
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!
Requirements
- 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.
Nice To Haves
- Bilingual a plus!
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.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
