Analytical Scientist (Contract) - HPLC/GLP

Trident Consulting; Irvine (CA); Vor Ort; USD 38.000 - 53.000; Vollzeit

Zusammenfassung

Trident Consulting is currently seeking an Associate Scientist for one of our industry-leading clients in Irvine, CA. The contract position runs for 12 months with a pay rate of $33/hour (W2).

The role involves operating analytical instruments (HPLC/UPLC, FTIR, Dissolution, UV-Vis), performing routine testing, analyzing data, and preparing technical reports, while ensuring GLP and safety compliance. You will support method development, validation, troubleshooting, and early-stage clinical

Qualifikationen

• Bachelor's degree in Analytical Chemistry, Pharmaceutical Sciences, Chemical Engineering, or related field.
• 1-2 years of hands-on analytical laboratory experience.
• Practical experience operating HPLC and knowledge of chromatographic principles and chemical analysis.
• Strong analytical, documentation, organizational, and communication skills.

Aufgaben

• Operate analytical laboratory instruments, including HPLC/UPLC, FTIR, Dissolution, and UV-Vis Spectrophotometers.
• Perform routine analytical testing, analyze data, and prepare technical reports.
• Support analytical method development, validation, troubleshooting, and optimization.
• Maintain accurate laboratory records and ensure GLP and laboratory safety standards compliance.
• Support new product development, formulation studies, and early-stage clinical research.

Kenntnisse

Analytical thinking

Documentation

Communication

Ausbildung

Bachelor's degree in Analytical Chemistry, Pharmaceutical Sciences, Chemical Engineering, or related field

Tools

HPLC

UPLC

FTIR

Dissolution

UV-Vis Spectrophotometers

Jobbeschreibung

Trident Consulting is currently seeking an Associate Scientist for one of our industry-leading clients in Irvine, CA. The contract position runs for 12 months with a pay rate of $33/hour (W2).

The role involves operating analytical instruments (HPLC/UPLC, FTIR, Dissolution, UV-Vis), performing routine testing, analyzing data, and preparing technical reports, while ensuring GLP and safety compliance. You will support method development, validation, troubleshooting, and early-stage clinical