Quality Engineering Co‑Op – MedTech R&D

Johnson & Johnson MedTech

Santa Clara (CA)

On-site

USD 37,000 - 84,000

Full time

13 hours ago
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Benefits offered by this job

Company sponsored medical benefits
Sick time benefits (40 hrs/yr; 56 hrs/
Retirement plan (pension)

Job summary

Johnson & Johnson MedTech is seeking a Quality Engineering Co-op in Santa Clara, CA for a 5- to 6-month term (January–June 2027). You will support product design verification/validation, develop lab testing, and perform statistical analyses under guidance from Quality Engineers.

Responsibilities include risk management documentation, collaboration with engineers and regulatory teams, and participation in on-site training courses.

Qualifications

  • Pursuing a Bachelor's or Master's in engineering fields (mechanical, biomedical, chemical, electrical or computer/Software).
  • Second year or above in the program at start of co-op/internship.
  • Familiar with basic statistics concepts/terminology.
  • Legally authorized to work in the U.S. without current or future visa sponsorship.
  • Willing to work full-time, 40 hours per week.

Responsibilities

  • Perform testing, experimentation, verification, and validation to support product design.
  • Assist in developing laboratory testing, interpreting data results, and recommending next steps.
  • Learn and perform various statistical analysis techniques.
  • Create and update risk management documents like FMEAs and quality plans.
  • Collaborate with cross-functional teams including Design, Development, Regulatory, Marketing and Clinical.

Skills

Statistics basics
Microsoft Office
Teamwork
Communication skills
Attention to detail
GPA 3.0

Education

Bachelor's or Master's in engineering

Tools

Minitab
Weibull/Reliasoft
SAS

Job description

Johnson & Johnson MedTech is seeking a Quality Engineering Co-op in Santa Clara, CA for a 5- to 6-month term (January–June 2027). You will support product design verification/validation, develop lab testing, and perform statistical analyses under guidance from Quality Engineers.

Responsibilities include risk management documentation, collaboration with engineers and regulatory teams, and participation in on-site training courses.

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