Quality Assurance Analyst I

Motion Recruitment; Fort Worth (TX); On-site; USD 39,000 - 50,000; Part time

Job summary

Motion Recruitment is seeking a Clinical and Scientific - Quality Assurance Analyst I for a ~4 month contract in Fort Worth, TX. The role supports QA Operations, monitors product quality, and ensures GxP compliance in aseptic pharmaceutical manufacturing.

The ideal candidate has a science degree, strong English communication, and proven ability to follow procedures in a fast-paced GMP environment. 12-hour day shifts, 4 on 4 off, with related SOP training and documentation responsibilities.

Qualifications

• Bachelore2 s degree in a science field and strong English communication skills.
• Detail-oriented, dependable, and quality-minded, with the ability to follow procedures in an aseptic pharmaceutical manufacturing environment.
• Comfortable with GxP documentation and cross-functional teamwork; aseptic, packaging, compounding, SAP, or LabVantage experience is a plus.

Responsibilities

• Support quality production by working with QA Operations and production teams.
• Monitor product quality, identify and escape non-conformances, and help resolve issues promptly.
• Maintain accurate records in paper and computerized systems while following SOPs, GxP requirements, and required training.

Skills

Bachelore2 s degree in science

Strong English communication

Detail-oriented

Quality-minded

Ability to follow procedures

GxP documentation

Cross-functional teamwork

Aseptic pharma environment familiarity

Education

Bachelore2 s degree in science

Tools

SAP

LabVantage

Job description

ExcitingQuality Assurance opportunity with anpharmaceutical manufacturing

Job Title: Clinical and Scientific - Quality Assurance Analyst I
Contract Duration:~4 Months (18 W)
Job Location: Ft Worth TX 76134
Day Shift: 12-hour shifts (6:00am-6:30pm CST) 4 days on, 4 days off

Required Skills & Experience

• Bachelor’s degree in a science field and strong English communication skills.


• Detail-oriented, dependable, and quality-minded, with the ability to follow procedures in an aseptic pharmaceutical manufacturing environment.


• Comfortable with GxP documentation and cross-functional teamwork; aseptic, packaging, compounding, SAP, or LabVantage experience is a plus.

What You Will Be Doing

• Support quality production by working with QA Operations and production teams.


• Monitor product quality, identify and escape non-conformances, and help resolve issues promptly.


• Maintain accurate records in paper and computerized systems while following SOPs, GxP requirements, and required training.