Quality Auditor - Scientific I (Onsite Contract, 1st Shift)

AGW; Elkhorn Precinct (NE); On-site; USD 29,000 - 41,000; Full time

Job summary

Aptask Global Workforce (AGW) is seeking a Quality Auditor - Scientific - I (Assistant) for an onsite, 12-month contract in Elkhorn, NE, supporting a Major Pharmaceutical Company. The role centers on reviewing completed production batch documents and providing quality compliance guidance.

Responsibilities include primary review of batch and raw material documentation, tracking reviews by target dates, assisting with archival tasks, and supporting inspections and investigations to uphold cGMP and

Qualifications

• High School Diploma with 3 years of work history or 1 year in a regulated industry.
• Experience in a regulated facility.
• Ability to conduct detailed, paper-based documentation reviews.
• Familiarity with compliance-driven processes and accurate recordkeeping.
• Onsite availability in Elkhorn, Nebraska for the first shift.

Responsibilities

• Perform primary review of completed production batch documents and raw material/printed material documentation
• Track and prioritize document reviews based on target release dates
• Provide documentation guidance from a quality compliance perspective
• Assist with document archival tasks
• Support inspections, investigations, and compliance actions
• Participate in Quality Compliance Inspections from regulatory agencies

Skills

Attention to detail

Regulatory compliance

Documentation review

On-site work

Education

High School Diploma

Bachelor's in Microbiology or Chemistry

Tools

SAP

Job description

Aptask Global Workforce (AGW) is seeking a Quality Auditor - Scientific - I (Assistant) for an onsite, 12-month contract in Elkhorn, NE, supporting a Major Pharmaceutical Company. The role centers on reviewing completed production batch documents and providing quality compliance guidance.

Responsibilities include primary review of batch and raw material documentation, tracking reviews by target dates, assisting with archival tasks, and supporting inspections and investigations to uphold cGMP and