QC Scientist

tsu.edu; Round Rock (TX); On-site; USD 41,000 - 52,000; Full time

Job summary

Texas Southern University in Round Rock, TX, seeks a QC Scientist (Analytical) to support Quality Control release testing. You will lead stability studies, optimize processes, and analyze reference materials for high-impact product launches.

Requirements include 2+ years with HPLC/GC, strong technical writing, and familiarity with ISO 9001/17025/17034. This role focuses on rigorous QC duties in a regulated lab environment.

Qualifications

• BS or MS in Chemistry, Analytical Chemistry, or related scientific discipline.
• 2+ years of hands-on industry experience utilizing HPLC and GC.
• Experience in ISO 9001, ISO 17025, or ISO 17034 environments.
• Strong technical writing abilities to document OOS reports, test methods, and validation protocols.

Responsibilities

• Perform QC release testing on finished products, raw materials, and analytical standards using HPLC and GC systems.
• Operate and maintain chromatographic detectors including UV-Vis, RI, ELSD, and FID.
• Draft, review, and process lab documentation such as OOS investigations, batch records, test specifications, and technical reports.
• Support product development, method validation, stability assessments, and tech transfer to the QC lab.
• Perform routine equipment qualifications, system troubleshooting, and routine lab maintenance.
• Ensure testing/documentation comply with ISO 9001, ISO/IEC 17025, ISO 17034 standards.

Skills

Analytical writing

Education

BS or MS in Chemistry/Analytical Chemistry

Tools

HPLC

GC

UV-Vis

RI

ELSD

FID

Job description

Title: QC Scientist
Location: Round Rock, TX
Pay: $30-38/hr
Contract: 12+ months

Must have: Chromotography, HPLC and GC

Summary

Are you looking to advance your analytical chemistry career with a premier global life sciences manufacturer? We are seeking a detail-oriented Scientist (Analytical) to support Quality Control release testing in Round Rock, TX. In this role, you will lead stability studies, optimize processes, and analyze reference materials to support high-impact product launches.

Responsibilities

• Perform QC release testing on finished products, raw materials, and analytical standards using HPLC and GC systems.
• Operate and maintain chromatographic detectors, including UV-Vis, RI, ELSD, and FID.
• Draft, review, and process lab documentation, including OOS investigations, batch records, test specifications, and technical reports.
• Support product development, method validation, stability assessments, and technical transfer to the QC laboratory.
• Perform routine equipment qualifications, system troubleshooting, and routine lab maintenance.
• Ensure all testing and documentation strictly comply with ISO 9001, ISO/IEC 17025, and ISO 17034 standards.

Qualifications

Required:

• BS or MS degree in Chemistry, Analytical Chemistry, or a related scientific discipline.
• 2+ years of hands-on industry experience utilizing HPLC and GC techniques.
• Demonstrated working knowledge of ISO 9001, ISO 17025, or ISO 17034 environments.
• Strong technical writing abilities to document OOS reports, test methods, and validation protocols.

Preferred:

• Prior analytical testing experience within GLP, GMP, or regulated life sciences manufacturing environments.
• Hands-on experience with equipment troubleshooting and mass balance techniques.