Quality Assurance Analyst

Motion Recruitment; Fort Worth (TX); On-site; USD 55,000 - 75,000; Full time

Job summary

Motion Recruitment is seeking a Clinical & Scientific Quality Assurance Analyst I to join our team in Fort Worth, TX. In this day shift role (4 days on/4 days off), you will monitor product quality during production, document deviations, and help resolve non-conformances within an aseptic pharmaceutical environment.

You will collaborate with QA Operations and Production to support quality manufacturing, compliance, and continuous improvement while following SOPs, GxP, and required trainings.

Qualifications

• 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.
• Aseptic, packaging, compounding, SAP, or LabVantage experience is a plus.

Responsibilities

• Monitor product quality throughout production and identify non-conformances.
• Maintain complete documentation in paper and computerized systems per SOPs and GxP requirements.
• Partner with QA Operations and Production to support quality manufacturing, compliance, and continuous improvement.

Skills

Detail-oriented

Quality-minded

English communication

Follow procedures

Education

Bachelor's degree in a science field

Tools

SAP

LabVantage

Microsoft Office

Job description

Now Hiring: Clinical & Scientific – Quality Assurance Analyst I

Day shift: 6:00 a.m.–6:30 p.m. CST, 4 days on / 4 days off

What we’re looking for

• Bachelor’s degree in a science field and strong English communication skills.
• Detail-oriented, dependable, and quality-minded, with the ability to follow procedures and make job‑related decisions in an aseptic pharmaceutical manufacturing environment.
• Able to stand and walk for extended periods; Microsoft Office skills are preferred. Aseptic, packaging, compounding, SAP, or LabVantage experience is a plus.

What you’ll be doing

• Monitor product quality throughout production and promptly identify, escape, and help resolve non‑conformances.
• Maintain complete, accurate documentation in paper and computerized systems while following SOPs, GxP requirements, and required training.
• Partner with QA Operations and Production teams to support quality manufacturing, compliance, and continuous improvement.