QA Chemist II

17h17 hours ago

Fujifilm

Carrollton, US · Full-time · $80,000 – $105,000

About this role

FUJIFILM Ultra-Pure Solutions, Inc. is a global leader in chemical solutions enabling the semiconductor industry. The QA Chemist II performs analytical testing on raw materials and finished products for composition and impurities. This role records quality results at our Carrollton, Texas facility.

Daily tasks include testing and approving raw materials, intermediates, and final products using lab equipment like GC, Karl Fischer titration, ICP-MS, and NVR. Complete and issue Certificates of Analysis. Investigate out-of-specification results and review process control charts.

Respond to deviations by assessing impact on product safety and quality. Perform instrument validation, troubleshooting, repair, and maintenance. Maintain laboratory upkeep, cleaning, waste disposal, and gas systems in a cross-functional team environment.

Ensure a safe and healthy work environment by following standards and complying with legal regulations. Develop, review, and update laboratory documents and procedures. Join state-of-the-art facilities supporting top-tier semiconductor manufacturers worldwide.

Requirements

BA/BS Chemical degree and minimum of 3-5 years of experience in the semiconductor or related field or in a production laboratory environment or master’s degree with 2 years of experience; PhD will also be considered
Instrumentation and analytical skills experience preferred - wet chemistry techniques, UV-Vis, GC/FID/TCD, IC, HPLC, GFAA, ICP/OES, ICP/MS, FTIR, GC/MS, and liquid particle counters
Ability to multi-task and handle change in priorities
Strong organization skills, good attention to detail, and the ability to function effectively as part of a cross functional team
Strong verbal and written communication skills
Excellent computer skills (Word, PowerPoint, Excel and statistical software tools)
Strong troubleshooting skills
Ability to speak Korean is a plus

Responsibilities

Test and approve raw materials, intermediates, and final products using lab equipment (e.g., GC, Karl Fischer titration, ICP-MS, NVR)
Complete and issue Certificates of Analysis (COA)
Investigate out of specification and out of control results
Review process control charts and take action as required
Develop, review, and update laboratory documents and procedures
Respond to deviations by assessing the impact on product safety and quality
Perform instrument validation, troubleshooting, repair, and maintenance
Maintain laboratory upkeep and cleaning, waste disposal, and gas maintenance