Quality Engineer

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The company built on breakthroughs.
Join us.

Corning is one of the world's leading innovators in glass, ceramic, and materials science. From the depths of the ocean to the farthest reaches of space, our technologies push the boundaries of what's possible.

How do we do this? With our people. They break through limitations and expectations- not once in a career, but every day. They help move our company,and the world, forward.

At Corning, there are endless possibilities for making an impact. You can help connect the unconnected, drive the future of automobiles, transform at-home entertainment, and ensure the delivery of lifesaving medicines. And so much more.

Come break through with us.

Corning's businesses are ever-evolving to best serve our customers, industries, and consumers. Today, we accelerate and transform life sciences, mobile consumer electronics, optical communications, display, automotive, and solar markets. We are changing the world with:

• Trusted products that accelerate drug discovery, development, and delivery to save lives
• Damage-resistant cover glass to enhance the devices that keep us connected
• Optical fiber, wireless technologies, and connectivity solutions to carry information and ideas at the speed of light
• Precision glass for advanced displays to deliver richer experiences
• Auto glass and ceramics to drive cleaner, safer, and smarter transportation
• Solar polysilicon, wafers, and innovative photovoltaic modules, enabling low-cost solar energy solutions

Corning is seeking a Quality Engineer II to support manufacturing operations and project teams across assigned product lines. Reporting to the Quality Engineering Supervisor, you will provide quality guidance, product disposition decisions, and statistical problem-solving expertise in support of new product introduction, process improvements, continuous improvement initiatives, and validation activities. This role involves up to 15% travel, with the potential for additional travel during the first six months.

Key Responsibilities

• Support Material Review Board (MRB) activities including blocked stock reviews, non-conforming product investigations, and customer complaint resolution; facilitate Failure Investigation Reports (FIR), Situation Analysis, and Health Hazard Evaluation with clear documentation of corrective actions
• Apply quality engineering tools - including Six Sigma, Failure Mode and Effects Analysis (FMEA), Design of Experiments (DOE), Measurement System Analysis (MSA), and validation protocol development - to support project teams and manufacturing operations; assist with Corrective and Preventive Action (CAPA) investigations
• Develop and revise quality plans covering incoming, in-process, and final inspection; implement inspection and metrology improvements; review and approve Project Design History Files and create technical process documentation
• Ensure compliance with regulatory requirements including ISO 13485, ISO 15378, FDA 21 CFR Part 820, and current Good Manufacturing Practices (cGMP); serve as a resource for internal audits supporting quality system compliance
• Monitor environmental and water monitoring programs including data trending, excursion identification, and corrective action oversight; manage from collection through results trending

Required Education & Experience

• Bachelor's degree in engineering, statistics, or a related technical discipline
• 3+ years of high volume manufacturing quality engineering experience, preferably in a regulated industry such as medical devices
• Knowledge of quality engineering tools including Six Sigma, FMEA, DOE, MSA, and validation methodology
• Thorough knowledge of regulatory requirements including ISO 13485, ISO 15378, FDA 21 CFR Part 820, and GDP/cGMP
• Proficiency in Minitab, Microsoft Project, and Microsoft Office applications
• Demonstrated technical writing skills with experience creating process documentation and quality plans
• Ability to make product disposition decisions and evaluate CAPA effectiveness

Desired Education & Experience

• Six Sigma certification (Green Belt or Black Belt)
• ASQ (American Society for Quality) Certified Quality Engineer (CQE)
• Experience in medical device or pharmaceutical manufacturing
• Familiarity with lean and continuous improvement methodologies

This position does not support immigration sponsorship.

The range for this position is $80,011.00-$ assuming full time status. Starting pay for the successful applicant is dependent…