Supplier Quality Engineering Coop

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.  We provide an inclusive work environment where each person is considered as an individual.  At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

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. 

• Build skills in quality data analysis, technical documentation, investigation support, supplier performance monitoring, and project management. 

• Learn how Quality, Engineering, Manufacturing, and Procurement collaborate to manage supplier and product risk. 

• Present project results and recommendations to Supplier Quality and cross-functional stakeholders. 

SUPERVISION / AUTHORITY 

This position has no supervisory responsibility. The co-op performs assigned work under close to general supervision, follows defined procedures, and receives regular coaching and review from a Supplier Quality Engineer or Quality Assurance manager. The co-op does not independently approve quality records, make final product disposition decisions, or represent the company as the accountable quality authority. 

ADDITIONAL POSITION REQUIREMENTS 

• Primarily onsite in Milpitas, California. 

• Occasional local or supplier-site travel may be requested when appropriate and approved. 

• Ability to work in office, laboratory, manufacturing, and warehouse environments as required, while following applicable safety and gowning requirements. 

Permanently authorized to work in the U.S., must not require sponsorship of an employment visa (e.g., H-1B or green card) at the time of application or in the future.  Students currently on CPT, OPT, or STEM OPT usually requires future sponsorship for long term employment and do not meet the requirements for this program unless eligible for an alternative long-term status that does not require company sponsorship.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation,  external applicants please contact us via https://www.jnj.com/contact-us/careers . Internal employees contact AskGS to be directed to your accommodation resource.

Additional Description for Pay Transparency: