QC Chemist, Semiconductor Materials Lab

FUJIFILM Electronic Materials U.S.A., Inc.

Mesa (AZ)

On-site

USD 56,000 - 73,000

Full time

3 days ago
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Job summary

FUJIFILM Electronic Materials, U.S.A., Inc. is seeking a QC Chemist at our Mesa, Arizona facility to serve as a Quality Control Specialist.

The role focuses on analyzing semiconductor materials in support of product qualification and laboratory processes. The candidate will review materials from raw to final product, investigate non-conformances, monitor stability charts, troubleshoot equipment, and update laboratory documents in line with Good Laboratory Practices.

Qualifications

  • Bachelor’s degree in Chemistry or related field.
  • 0–1 years of experience in a production lab environment.
  • Experience with laboratory instrumentation and Good Laboratory Practices.
  • Statistical software experience preferred.
  • Candidate must be able to multi-task and adapt to changing priorities.
  • Good communication skills across functional groups.
  • Must be able to work first or second shift, including weekends/holidays.
  • Post-offer drug screening required; safety-sensitive role.

Responsibilities

  • Analyze raw materials, intermediates, and final products per company procedures.
  • Investigate non-compliance test results to ensure specifications.
  • Review long-term stability charts to ensure equipment remains fit-for-use.
  • Troubleshoot and perform maintenance activities on equipment.
  • Review and update laboratory documents to comply with GLP.

Skills

Communication skills
Multi-tasking
Problem solving
Safety-conscious

Education

BA/BS in Chemistry or related degree

Tools

ICP/MS
GC/MS
UV-Vis
HPLC

Job description

FUJIFILM Electronic Materials, U.S.A., Inc. is seeking a QC Chemist at our Mesa, Arizona facility to serve as a Quality Control Specialist.

The role focuses on analyzing semiconductor materials in support of product qualification and laboratory processes. The candidate will review materials from raw to final product, investigate non-conformances, monitor stability charts, troubleshoot equipment, and update laboratory documents in line with Good Laboratory Practices.

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