Quality Assurance Auditor
Job in
South Brunswick, Middlesex County, New Jersey, USA
Listed on 2026-01-12
Listing for:
Eurofins BioPharma Product Testing North America
Full Time
position Listed on 2026-01-12
Job specializations:
-
Quality Assurance - QA/QC
Quality Technician/ Inspector, Quality Control / Manager, QA Specialist / Manager
Job Description & How to Apply Below
Eurofins Bio Pharma Product Testing North America – Quality Assurance Auditor
3 days ago – Position is full‑time, Monday‑Friday 8am‑5pm. Candidates located near South Brunswick, NJ are encouraged to apply.
CompensationBase pay range: $22.50/hr – $25.50/hr additional benefits include comprehensive medical, dental and vision coverage, life and disability insurance, 401(k) with company match, paid vacation and holidays.
Responsibilities- Assist in the performance of all Quality Assurance functions as outlined in GLPs and PSL SOPs.
- Support the Quality Assurance Director during inspections by EPA, FDA or clients; prepare records and assemble copies of documents requested by inspectors when advanced notice is given and approval is obtained.
- Conduct in‑process study inspections and general facility inspections in the toxicology and chemistry laboratories as directed.
- Audit raw data and proofread reports and tables against raw data for accuracy and for typing corrections; audit final reports to verify corrections.
- Amend and update Standard Operating Procedures as required using word processing system; file all QAU‑related paperwork as directed.
- Select intervals for inspection for any regulatory test under the auditor's responsibility or as directed by QA Director, Laboratory Director, or President; perform such inspections in accordance with the test schedule; notify Study Director or QA Director when inspection falls outside normal working hours to arrange a suitable time.
- Ability to safely wear a respirator required.
- Other duties as assigned.
- QA auditor experience in a laboratory regulated by FDA/EPA GLP standards; experience in other quality standards such as cGMP or GCP considered.
- Experience with acute toxicology, analytical chemistry, and/or general laboratory procedures preferred; BS degree in biology, toxicology, animal science or related field and/or AALAS certification at the Technician level preferred.
- Strong integrity, high sense of responsibility, attention to detail, well organized, tactful; able to work independently and maintain all records, documents and schedules associated with quality assurance procedures and studies.
- Excellent written communication skills; proficiency with MS Word and Excel required. Current tetanus vaccination required if accessing the vivarium.
South Brunswick, NJ. Eurofins USA Bio Pharma Services is a Disabled and Veteran Equal Employment Opportunity employer. For inquiries, visit Eurofins Bio Pharma Product Testing North America
.
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