Quality Control Chemist II, Pharma CDMO in Houston TX
Overview
Quality Control Chemist II will own analytical testing across raw materials, in‑process, and finished products at a premier CDMO. The role involves using analytical instrumentation, maintaining equipment, and ensuring cGMP compliance within a collaborative pharmaceutical manufacturing environment. You will review peer data and support calibration and qualification activities to sustain quality for the full drug product lifecycle.
What You'll Do10
- 1Build and perform analytical testing of raw materials, in‑process samples, and finished products with accurate documentation.
- 2Utilize analytical instrumentation and assist with instrument operation under supervision to generate reliable data.
- 3Ensure cGMP compliance and follow standard operating procedures to maintain quality systems.
- 4Peer review data generated by fellow technicians to uphold data integrity.
- 5Maintain and troubleshoot laboratory equipment and analytical instrumentation within your experience level.
- 6Perform and assist with equipment calibrations and qualifications to validate measurement systems.
- 7Assist with method transfers, troubleshooting, and data review to support batch release.
- 8Collaborate with cross‑functional teams to support product quality and regulatory readiness.
- 9Support continuous improvement initiatives in the QC lab to enhance efficiency and data quality.
- 10Complete other related duties as required to ensure smooth QC operations.
Requirements3
- 1Bachelor’s degree in Chemistry
- 22+ years of experience in a professional chemistry laboratory
- 32+ years of experience with analytical instrumentation such as HPLC, GC, CE, ICP, FTIR, TOC, MS, and dissolution apparatus
Salary Insight
$52 - $67k per year
Location
Required Skills
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