Quality Control Chemist

Johnson & Johnson; Austin (TX); On-site; USD 85,000 - 120,000; Full time

Benefits offered by this job

Restaurant d'entreprise

Indemnités de stage/alternance

Job summary

Johnson & Johnson in Austin, TX seeks an analytical chemist to perform testing of finished products, raw materials, and in-process samples using HPLC and GC. You will develop methods, support validations, and contribute to stability assessments.

You will investigate out-of-spec results, prepare technical documentation, and collaborate with cross-functional teams to drive quality improvements in a regulated environment.

Qualifications

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

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.

Skills

Analytical testing

HPLC/GC operation

Method development

Troubleshooting

Technical writing

Team collaboration

Equipment qualifications

Process improvement

OOS investigation

Education

BS or MS in chemistry or life sciences

Tools

HPLC system

GC system

Job description

• 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.
• 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.