Pharma QA Analyst I — Aseptic QC, 4-Month Contract

Motion Recruitment

Fort Worth (TX)

On-site

USD 39,000 - 50,000

Part time

8 days ago

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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

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.

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