Specialist, Quality Assurance
About The Position
Entegris is currently seeking a Specialist, Quality Assurance to join our Chemical Mechanical Pads Pads (CMP) team, within the Formulated Solutions business unit. This position will be based at our Aurora, Illinois facility. In this role, you will support the execution and documentation of core quality programs that ensure stable manufacturing processes and customer satisfaction. You will work closely with operations, engineering, and quality team members to support process control, FMEA and product control plan maintenance, and other quality programs, with a strong emphasis on clear, accurate documentation and data review.
Requirements
- Bachelor’s degree in Engineering, Quality, Manufacturing, Industrial Engineering, or a related technical field
- 3+ years of experience in a manufacturing, quality, or engineering environment
- Foundational knowledge of Statistical Process Control (SPC), root cause analysis and CAPA, FMEA and Product Control Plans
- Strong written documentation skills with attention to detail
- Working knowledge of Microsoft Office (Excel, Word, PowerPoint)
- Ability to analyze data, summarize findings, and communicate clearly with technical and non‑technical audiences
- Willingness to learn internal quality systems, tools, and procedures, as well as basic manufacturing processes
- Ability to work onsite at the Aurora facility
Responsibilities
- Support Out-of-Control Action Plans (OCAPs) and other internal investigations and responses by gathering data, documenting findings, and tracking Corrective and Preventive Actions (CAPAs) to completion.
- Prepare and maintain Statistical Process Control (SPC) trend review summaries, highlighting process stability, process shifts, and opportunities for improvement.
- Complete control limit reviews and updates, including data preparation, statistical summaries, and documentation of proposed changes
- Maintain and update Failure Modes and Effects Analyses (FMEAs) and process control plans to reflect current process controls, inspection methods, and learnings from quality issues or process changes.
- Author, revise, and maintain quality documentation including reports, summaries, and supporting records in accordance with site and corporate procedures
- Coordinate internal audit scheduling and track closure of CAPA
- Participate in cross‑functional meetings related to site quality performance, trend reviews, and continuous improvement activities
- Support audits and reviews by ensuring documentation is complete, accurate, and readily accessible
- Complete required training, administrative activities, and continuous improvement participation as assigned
Benefits
- Annual bonus eligibility
- Progressive paid time off policy that empowers you to take the time you need to recharge
- Generous 401(K) plan with an impressive employer match with no delayed vesting
- Excellent health, dental and vision insurance packages to fit your needs
- Education assistance to support your learning journey
- A values-driven culture with colleagues that rally around People, Accountability, Creativity and Excellence
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
