Supplier Quality Engineering Coop

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Job Function:

Career Programs

Job Sub Function:

Non-LDP Intern/Co-Op

Job Category:

Career Program

All Job Posting Locations:

Milpitas, California, United States of America

Job Description:

The Supplier Quality Engineering Co-op supports the Supplier Quality team in maintaining and improving the quality of materials, components, and services provided by external suppliers. Working under the guidance of experienced Supplier Quality Engineers, the co-op will contribute to supplier performance monitoring, quality data analysis, documentation, investigations, qualification activities, and continuous improvement projects in a regulated medical device environment.

This position provides practical experience applying engineering, quality, and problem-solving principles while working with cross-functional teams and suppliers. The co-op is expected to follow company procedures, protect confidential information, and support environmental, health, and safety objectives.

ESSENTIAL FUNCTIONS / RESPONSIBILITIES

• Support cross-functional Supplier Quality projects in accordance with established procedures and applicable regulatory requirements.

• Collect, organize, analyze, and present supplier quality data, including nonconformance, defect, delivery, audit, and performance information.

• Create and maintain supplier scorecards, trend charts, trackers, and concise status reports using Excel, PowerPoint, and other approved systems.

• Assist Supplier Quality Engineers with supplier and process qualification records, specifications, inspection plans, control plans, and validation documentation.

• Support supplier-related nonconformance investigations by gathering evidence, documenting problem statements, reviewing records, and tracking corrective actions.

• Participate in root cause analysis and continuous improvement activities using structured problem-solving tools under the direction of a Supplier Quality Engineer.

• Assist with preparation for supplier audits, quality reviews, and supplier meetings; document actions and follow up with assigned owners.

• Review quality records and technical documentation for completeness, accuracy, and alignment with approved requirements.

• Help identify process variation, recurring defects, overdue actions, and other potential supplier or supply chain risks for team review.

• Track project schedules, commitments, and due dates; promptly communicate risks, gaps, and support needed.

• Collaborate with Quality, Engineering, Manufacturing, Procurement, and other functions to complete assigned work.

• Perform other Supplier Quality and Quality Assurance activities appropriate to the student’s education, experience, and level of supervision.

QUALIFICATIONS

• Currently enrolled in an accredited bachelor’s or master’s degree program in Engineering, Data Science, Quality, Manufacturing, or a related science or technical field.

• Available for the full co-op assignment period and able to work the schedule defined for the position.

• Basic understanding of engineering, manufacturing, statistics, or quality principles through coursework or project experience.

• Proficiency with Microsoft Excel, Word, and PowerPoint; ability to organize data and communicate results clearly.

• Strong attention to detail, organization, follow-through, and willingness to learn.

• Ability to work effectively with team members from different functions and backgrounds.

• Clear written and verbal communication skills.

Preferred Qualifications

• Coursework or project experience in quality engineering, statistics, manufacturing processes, mechanical or electrical systems, or medical devices.

• Exposure to problem-solving methods such as 5 Whys, fishbone diagrams, Pareto analysis, process mapping, or failure mode and effects analysis.

• Experience analyzing data, creating dashboards, or using statistical or visualization tools.

• Interest in supplier management, regulated products, product development, or manufacturing operations.

LEARNING AND DEVELOPMENT OPPORTUNITIES

• Gain hands-on exposure to supplier quality management in a regulated medical device environment.

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