7 дней назад
Production Engineering Co-op (MedTech)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Production Engineering Co-op (MedTech): Supporting the design, improvement, validation, and transfer of medical device manufacturing processes, tooling, and fixtures with an accent on Lean and Six Sigma analysis, process documentation, and product quality. Focus on executing process validations, qualifying tooling through IQ/OQ/PQ and capability studies, investigating failures, and improving production yield.
Location: Danvers, Massachusetts, United States; onsite
Company
Johnson & Johnson MedTech develops healthcare and medical technology solutions, including products that support less invasive treatment and improved patient care.
What you will do
- Support the design, development, improvement, and validation of manufacturing processes, tooling, and fixtures.
- Provide production-floor support and contribute to defect reduction, productivity improvements, process performance, yield, and product quality.
- Support commercial production, product changes, production transfers, and cross-functional work with Operations, Product Development, and Quality Assurance.
- Develop and maintain process documentation, including assembly and test procedures, routers, travelers, bills of materials, process flows, and process FMEAs.
- Assist with validation plans, protocols, reports, IQ/OQ/PQ activities, Gage R&R studies, capability studies, and design of experiments.
- Participate in failure investigations and corrective actions while supporting Good Manufacturing Practices, FDA Quality System Regulations, and applicable ISO standards.
Requirements
- Junior, senior, or graduate student pursuing an engineering degree.
- Knowledge of Lean, Six Sigma, Kaizen, and continuous improvement methods.
- Ability to communicate clearly, prioritize work, and complete tasks with limited direct supervision.
- Proficiency in Microsoft Office; working knowledge of SAP is desired.
- Must be permanently authorized to work for any employer in the United States.
- Employment visa sponsorship is not available now or in the future; applicants requiring H-1B, green card, or other company sponsorship are not eligible.
Nice to have
- Prior work experience, especially in medical devices.
- Lean or Six Sigma Green Belt certification.
Culture & Benefits
- Work with global, cross-functional Operations, Product Development, and Quality Assurance teams.
- Contribute to healthcare innovation and medical technology products.
- Inclusive work environment focused on diversity, dignity, and equal opportunity.
Hiring process
- The program runs from January 11, 2027, through June 25, 2027.
- An inclusive interview process and reasonable accommodation support are available for applicants with disabilities.
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