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Quality Control Chemist

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Onsite

Quality Control Chemist

Johnson & Johnson

Quality Control Chemist

Skills

Process Improvement

21 days ago

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Important information


Contract type:

Permanent

Location:

Austin, TX, USA

Work mode:

Onsite

Published on:

1 October 2026

What they need


Key responsibilities:

  • Perform analytical testing of finished products, raw materials, in-process samples, and custom analytical services.
  • Operate HPLC, GC, and chromatographic detectors while troubleshooting and maintaining analytical systems.
  • Develop methods, support validations and technical transfers, and conduct stability assessments.
  • Investigate out-of-specification results and prepare reports, specifications, batch records, and technical documentation.
  • Collaborate with scientists, technicians, and project teams to manage tasks, timelines, resources, and project updates.
  • Participate in equipment qualifications, colleague training, and process improvement initiatives.

Basic qualifications:

  • BS or MS in chemistry or a related life science field.
  • 4+ years of related industry experience.
  • Demonstrated knowledge of analytical methods and analytical results interpretation.
  • Experience operating HPLC and GC instrumentation.
  • Excellent verbal communication and technical writing skills.

Preferred qualifications:

  • Knowledge of ISO 9001, ISO/IEC 17025, and ISO 17034 requirements.
  • Experience in GLP, GMP, or ISO-regulated environments.
  • Knowledge of quality systems in medical device, pharmaceutical, or clinical industries.
  • Experience with UV-Vis, RI, ELSD, FID, or other chromatographic detectors.
  • Experience with mass balance techniques traceable to primary pharmacopoeias.

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