The Analytical Quality Control (QC) Manager will be responsible for overseeing and managing quality control processes within the Operations Support team, with a specific focus on analytical methods to support certificate of analysis (COA) reporting. This role ensures that all products meet the required quality standards and comply with semiconductor industry regulations. The Analytical QC manager will work closely with other departments to implement and maintain quality control systems and processes. This position reports to the Analytical Director, within the Operations Support Department, but is dotted line to the Quality Department. While supervising individuals is not a primary responsibility at this time, it is expected to be part of the role in the future.
Primary Responsibilities:
Develop and implement quality control policies and procedures to ensure. compliance with semiconductor industry standards and regulations, with a focus on analytical methods for COA reporting.Review current chemical QC processes and implement CIPs.Collaborate with cross-functional teams, including production, engineering, quality, and customer service, to address quality issues and implement corrective actions.Conduct regular audits and inspections of products and processes to identify areas for improvement and ensure adherence to quality standards.Maintain and update QC documentation, including standard operating procedures (SOPs), work instructions, and quality records.Analyze quality data and trends to identify root causes of failures and implement preventive measures.Lead and participate in continuous improvement initiatives to enhance product quality and operational efficiency.Ensure that all customer re-certification requirements are met and maintain effective communication with the Quality and Customer teams regarding quality-related matters.Develop, validate, and maintain analytical methods/systems to support COA reporting.Oversee the chemical QC process, including scheduling, training, and analytical lab operation.Develop and maintain KPIs for chemical QC.Occasional commute to Beaverton office/lab.Other duties as assigned.Key Qualifications:
Bachelor’s degree in chemistry, engineering, quality management, or a related field (or equivalent experience).Minimum of 2 years of experience in managing a technical team and 4+ years QA/QC management experience, ideally in a chemical manufacturing or semiconductor environment.Deep understanding of safe chemical practices, safe practices around chemical manufacturing equipment, and quality requirements for the semiconductor industry.Ability to read SDSs and understand the chemical hazards to yourself and the environment.Proficiency in analytical chemistry, including sample preparation, routine analysis (including but not limited to GC-MS, ICP-OES, ICP-MS, NMR, LC-MS, and other), and quantitative analysis.Strong knowledge of quality control principles, methodologies and tools such as Statistical Process Control (SPC), Measurement System Analysis (MSA), Change Control/Management, Material Review Board (MRB).Expertise in data analysis and statistical skills, utilizing JMP to analyze quality data, identify trends, and implement preventive measures.Ability to mentor a technical team with strong analytical chemistry and QC/QA background.Effective communication and interpersonal skills.Proficiency in using quality management software and tools, including MS Suite, JMP, MES (Manufacturing Execution System), and LIMS.Strong problem-solving skills to identify root cause of issues from chemical analyses.Experience in ISO certification and KPI management.Responsiveness and flexibilityProject management and planningCreative and innovative with a customer focusAbility to successfully complete a pre-employment drug test.Physical Requirements:
Ability to sit or stand for long periods of time.Ability to lift 40 pounds from floor to table height.Ability to use a keyboard and mouse for computer data entry and/or analysis, and for presenting data.Ability to wear standard cleanroom attire in areas that require it.Ability to wear standard PPE in areas that require it.Ability to use a glovebox with thick rubber gloves to accurately pour, pipet, mix, and handle chemicals in small vials or bottles.40 hours/week or more may vary depending on the needs of the department; occasional weekend may be required.100% of work hours are expected to be onsite.Domestic day travel is estimated at 10-20% with travel occurring weekly (2-4 Beaverton office trips per month).Compensation and Benefits:
Inpria offers competitive compensation including a bonus and an excellent benefits package:
Group health, dental, and vision insurance with family coverage.Life insurance, short-term disability, and long-term disability aid for by Inpria.401(k) plan with employer matching contributions.Paid holidays, vacation, and sick leave.About Inpria:
Inpria Corporation is the world leader in metal oxide photoresist design, development, and manufacturing. Inpria’s EUV photoresists enable semiconductor manufacturers to realize the full potential of EUV lithography.
Nestled against the foothills of the coast range, Corvallis, OR is consistently ranked among the country's most livable and family-friendly towns, offering excellent outdoor recreation activities in the nearby Cascade Mountains and Oregon coast.
Equal Opportunity Statement:
Inpria is an equal-opportunity employer. At Inpria, we recognize that diversity of thought enhances innovation and problem-solving. Inpria is dedicated to creating an inclusive work environment where employees feel respected, valued, and empowered. We embrace and celebrate the unique experiences, perspectives, and cultural backgrounds each employee brings to our workplace.
Learn more at www.inpria.com