Semiconductor QC Chemist - Precision Lab & Analysis

FUJIFILM Electronic Materials U.S.A., Inc.; Pueblo (CO); On-site; USD 60,000 - 65,000; Full time

Job summary

FUJIFILM Electronic Materials, U.S.A., Inc. in Pueblo, CO is seeking a QC Chemist to analyze semiconductor materials for product qualification and support QC laboratory processes.

The role includes testing raw materials, intermediates, and final products following established procedures. Responsibilities include investigating non-conformances, reviewing stability charts, performing routine and automated tests, and maintaining accurate documentation in line with Good Laboratory Practices.

Qualifications

• BA/BS in Chemistry or related field required.
• 0–1 years of experience in a production lab environment.
• Instrumentation experience preferred with tools such as ICP/MS, GC/MS, UV-Vis, GC/FID/TCD, IC, HPLC, GFAA, ICP/OES, or liquid particle counters.

Responsibilities

• Analyze raw materials, intermediates, and final products following company procedures.
• Investigate non-compliance test results to assure the substance meets specifications.
• Review long-term stability charts to ensure equipment meet fit-for-use criteria.
• Perform troubleshooting, repairs and maintenance activities.
• Update laboratory documents in line with Good Laboratory Practices.
• Complete a high volume of work and perform tests per procedures.
• Adhere to safety procedures and participate in EH&S training.

Skills

Communication skills

Multi-tasking

Team collaboration

Education

BA/BS in Chemistry

Tools

MS Office

ICP/MS

GC/MS

UV-Vis

GC/FID/TCD

IC

HPLC

GFAA

ICP/OES

Job description

FUJIFILM Electronic Materials, U.S.A., Inc. in Pueblo, CO is seeking a QC Chemist to analyze semiconductor materials for product qualification and support QC laboratory processes.

The role includes testing raw materials, intermediates, and final products following established procedures. Responsibilities include investigating non-conformances, reviewing stability charts, performing routine and automated tests, and maintaining accurate documentation in line with Good Laboratory Practices.