Supplier Quality Co-op: MedTech Data & QA

Johnson & Johnson Co.; Milpitas (CA); On-site; USD 37,000 - 84,000; Full time

Benefits offered by this job

Medical benefits (Co-ops/Interns)

Sick time benefits

Retirement plan

Job summary

Johnson & Johnson seeks a Supplier Quality Co-op in Milpitas, California, working under the guidance of experienced engineers to improve supplier quality in a regulated medical device environment.

The role involves data analysis, documentation, and cross-functional collaboration with Quality, Engineering, Manufacturing, and Procurement teams. Onsite work, CPT/OPT considerations apply, with opportunities to learn quality data analysis and project management.

Qualifications

• Currently enrolled in an accredited bachelor's or master's degree program in Engineering, Data Science, Quality, Manufacturing, or a related field.
• Available for the full co-op assignment period and able to work the schedule defined for the position.
• Proficiency with Microsoft Excel, Word, and PowerPoint; ability to organize data and communicate results clearly.

Responsibilities

• Support cross-functional Supplier Quality projects following established procedures and regulatory requirements.
• Collect, organize, analyze, and present supplier quality data (nonconformance, defects, delivery, audits, performance).
• Create and maintain supplier scorecards, trend charts, trackers, and concise status reports using Excel, PowerPoint, and approved systems.
• Assist with supplier and process qualification records, specifications, inspection plans, control plans, and validation documentation.
• Support supplier-related nonconformance investigations and track corrective actions.

Skills

Excel proficiency

Word proficiency

PowerPoint proficiency

Analytical skills

Education

Bachelor’s or Master’s in Engineering/Quality/Data Science/Manufacturing

Tools

Excel

Word

PowerPoint

Job description

Johnson & Johnson seeks a Supplier Quality Co-op in Milpitas, California, working under the guidance of experienced engineers to improve supplier quality in a regulated medical device environment.

The role involves data analysis, documentation, and cross-functional collaboration with Quality, Engineering, Manufacturing, and Procurement teams. Onsite work, CPT/OPT considerations apply, with opportunities to learn quality data analysis and project management.