Quality Control Specialist - HPLC/GC (Round Rock, TX)

ManpowerGroup

Round Rock (TX)

On-site

USD 48,000 - 52,000

Full time

3 days ago
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Benefits offered by this job

Medical
Dental
Vision
401(k)
Temp-to-perm

Job summary

ManpowerGroup is seeking a Quality Control Expert for a Round Rock, TX role in a leading Life Sciences and Biotechnology company. You will support analytical testing, product development, and quality assurance within the Quality Control Laboratory.

The candidate should have a BS or MS in Chemistry or related Life Sciences, 2+ years in an analytical lab, hands-on HPLC/GC experience, and familiarity with GMP/GLP/ISO environments. Strong technical writing and problem-solving are essential.

Qualifications

  • BS or MS in Chemistry or a related Life Sciences field.
  • 2+ years of industry experience in an analytical lab.
  • Hands-on experience with chromatography (HPLC/GC).
  • Experience in GMP/GLP/ISO or other regulated environments.
  • Strong technical writing and analytical problem-solving skills.

Responsibilities

  • Perform analytical testing of finished products, raw materials, and in-process samples using HPLC and GC.
  • Conduct stability studies and support product development, validation, and tech transfer.
  • Investigate OOS results and assist with root-cause analysis.
  • Prepare technical reports, batch records, test specifications, and lab documentation.
  • Troubleshoot, maintain, and qualify analytical instrumentation while ensuring compliance.

Skills

Analytical thinking
Attention to detail
Technical communication

Education

Bachelor's or Master’s in Chemistry or related Life Sciences

Tools

HPLC
GC

Job description

ManpowerGroup is seeking a Quality Control Expert for a Round Rock, TX role in a leading Life Sciences and Biotechnology company. You will support analytical testing, product development, and quality assurance within the Quality Control Laboratory.

The candidate should have a BS or MS in Chemistry or related Life Sciences, 2+ years in an analytical lab, hands-on HPLC/GC experience, and familiarity with GMP/GLP/ISO environments. Strong technical writing and problem-solving are essential.

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