Quality Assurance Analyst I

Kelly Services; Fort Worth (TX); On-site; USD 34,000 - 55,000; Full time

Job summary

Kelly Services is recruiting for a Clinical and Scientific - Quality Assurance Analyst I in Fort Worth, TX. This 4-month contract role supports QA Operations and production teams to ensure product quality and adherence to GxP requirements.

The candidate will maintain records and follow SOPs, with experience in aseptic manufacturing and cross-functional teamwork. The position requires a Bachelor's degree in a science field, strong English communication, and familiarity with SAP or LabVantage.

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.
• 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 elevate non-conformances, and help resolve issues promptly.
• Maintain accurate records in paper and computerized systems while following SOPs, GxP requirements, and required training.

Skills

English communication

Detail oriented

GxP documentation

Cross-functional teamwork

Aseptic manufacturing awareness

Education

Bachelor’s degree in a science field

Tools

SAP

LabVantage

Job description

Exciting Quality Assurance opportunity with an pharmaceutical 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 elevate non-conformances, and help resolve issues promptly.

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

Motion Recruitment Partners (MRP) is an Equal Opportunity Employer. All applicants must be currently authorized to work on a full-time basis in the country for which they are applying, and no sponsorship is currently available. Employment is subject to the successful completion of a pre-employment screening. Accommodation will be provided in all parts of the hiring process as required under MRP’s Employment Accommodation policy. Applicants need to make their needs known in advance.