Quality Engineering Intern

Johnson & Johnson • San Jose, CA

10d • Onsite

About The Position

As a Co-op/Intern in the Quality Engineering organization, you will have the chance to use state-of-the-art tools and take advantage of training courses offered on-site. You will perform testing, experimentation, verification, and validation to support product design. You will also assist in developing laboratory testing, interpreting data results, and recommending next steps. Additionally, you will learn and perform various statistical analysis techniques, create and update risk management documents like FMEAs, Quality plans, and complaint analyses, and strengthen communication and leadership skills. You will meet with Quality management to discuss risks and opportunities for the respective projects.

Requirements

• Candidates must be enrolled in an accredited College/University pursuing a Bachelor’s or Master’s degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering, Electrical Engineering, Computer/Software Engineering or a related field.
• Candidates must be in their third year or above in school at the start of the co-op/internship.
• Candidates must be familiar with basic statistics concepts/terminology.
• Candidates must be available to work Full-time. 40 hours per week.
• Candidates must be legally authorized to work in the United States and not require sponsorship for employment visa status (e.g. H1-B status) now or in the future.
• Candidates must be detail-oriented, highly organized and able to manage multiple tasks.
• Candidates must have the ability to work independently as well as on a team.
• Candidates must to be proficient with Microsoft Office (Word, Excel, Power Point) and have strong oral and written communication skills.
• Candidates must have a minimum G.P.A. of 2.8.

Nice To Haves

• Demonstrated leadership/participation in campus programs and/or community service activities.
• Previous quality engineering related experiences.
• Knowledge of FDA or regulatory guidance.
• Medical related experience (previous co-op at medical device company, working volunteering at a hospital, etc.).
• Advanced familiarity with statistics concepts/terminology (either from previous co-ops or classwork).
• Failure analysis/root cause understanding.
• 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.

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, Quality plans, and complaint analyses.
• Strengthen communication and leadership skills.
• Meet with Quality management to discuss risks and opportunities for the respective projects.
• Work in Operations Quality and Supplier Quality Engineering.
• May also work on projects for the equipment/calibration team.
• Report directly to, and receive assignments from, the team Quality Manager while also working with the broader team for additional assignments.
• Specific projects may include: Supplier Change Notification Process Enhancements, Implementation of OneASL, Calibration management systems, and/or participating in process validation activities for new products.

Benefits

• Company sponsored employee medical benefits
• Sick time benefits: up to 40 hours per calendar year; for employees who reside in the State of Washington, up to 56 hours per calendar year.
• Eligible to participate in the Company’s consolidated retirement plan (pension).

What This Job Offers

• Job Type: Full-time
• Career Level: Intern