Pharma Quality Auditor – Batch Release & Compliance (Hybrid)

Johnson Service Group, Inc.; Rahway (NJ); Hybrid; USD 100,289,000 - 111,751,000; Full time

Benefits offered by this job

Medical

Dental

Vision

Life insurance

Short-term disability

401(k)

Weekly pay

More

Job summary

Johnson Service Group (JSG) is recruiting a Quality Auditor for a two-year contract in Rahway, NJ. The role will involve on-site work three days per week with hybrid flexibility after training, and a pay rate of $35–$39 per hour.

The ideal candidate holds a science or engineering degree and at least three years in pharma/regulated environments, with strong documentation and QA experience, including batch review and GMP compliance.

Qualifications

• Bachelor's degree in a scientific or engineering discipline required.
• Minimum 3 years of experience in pharmaceutical, biotech, or regulated industry, focusing on batch disposition, QA, or GMP environments.
• Experience reviewing batch records, COAs, investigations, and regulated documents.
• Familiarity with GMP regulations, regulatory compliance, and quality systems.
• Proficiency with Microsoft Office (Word, Excel, PowerPoint, Teams) and SAP.

Responsibilities

• Review batch records, COAs, investigations, and other quality documents to ensure compliance.
• Make independent decisions on batch release or rejection based on reviews.
• Support quality system activities such as audits, deviations, CAPAs, and risk management.
• Prepare and document data to support continuous quality improvement initiatives.
• Collaborate with quality, lab, manufacturing, and warehouse staff daily.
• Assist in audit materials and site readiness activities.
• Develop, review, or update GMP procedures and standards.

Skills

Quality auditing

Attention to detail

Problem solving

Multitasking

MS Office

Education

Bachelor's degree in science or engineering

Tools

SAP

Veeva

Job description

Johnson Service Group (JSG) is recruiting a Quality Auditor for a two-year contract in Rahway, NJ. The role will involve on-site work three days per week with hybrid flexibility after training, and a pay rate of $35–$39 per hour.

The ideal candidate holds a science or engineering degree and at least three years in pharma/regulated environments, with strong documentation and QA experience, including batch review and GMP compliance.