Entry-Level Quality Lab Technician - GMP & Data Entry

ApTask Global Workforce; Wilson (NC); On-site; USD 33,000 - 55,000; Full time

Benefits offered by this job

Medical

Dental

Vision

Sick Pay

Job summary

ApTask Global Workforce (AGW) is seeking an Assistant Quality Specialist – I for an onsite 12-month contract with a major pharmaceutical company in Wilson, NC. The role focuses on routine laboratory testing of incoming components in a GMP environment, with data entry, investigations, and basic instrumentation troubleshooting.

The ideal candidate has an science/engineering background (or equivalent) and a willingness to learn, with familiarity in GMP documentation and teamwork.

Qualifications

• B.A./B.S. degree in Science or Engineering, OR an Associate degree with 3 years of pharmaceutical experience, OR a high school diploma with 5 years of pharmaceutical experience
• Good knowledge of GMP documentation
• Ability to quickly learn new processes, procedures, and equipment
• Good team mindset

Responsibilities

• Perform routine laboratory testing of incoming components
• Utilize testing equipment including calipers, Magna Mike, FTIR, and balances
• Enter data into Labware
• Participate in investigations and root cause analysis sessions
• Conduct minimal troubleshooting of instrumentation issues
• Participate in the daily tier process

Skills

GMP documentation

Team mindset

Fast learner

Education

B.A./B.S. in Science or Engineering

Associate degree + 3 years pharma

High school diploma + 5 years pharma

Tools

Calipers

Magna Mike

FTIR

Balances

Labware

SAP

GLIMS

Job description

ApTask Global Workforce (AGW) is seeking an Assistant Quality Specialist – I for an onsite 12-month contract with a major pharmaceutical company in Wilson, NC. The role focuses on routine laboratory testing of incoming components in a GMP environment, with data entry, investigations, and basic instrumentation troubleshooting.

The ideal candidate has an science/engineering background (or equivalent) and a willingness to learn, with familiarity in GMP documentation and teamwork.