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Production Engineering Co-op

Job in Danvers, Essex County, Massachusetts, 01923, USA
Listing for: Johnson Johnson
Full Time position
Listed on 2026-10-11
Job specializations:
  • Engineering
    Quality Engineering, Process Engineer, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 28000 - 39000 USD Yearly USD 28000.00 39000.00 YEAR
Job Description & How to Apply Below

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 Med Tech, 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

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.

Job Function:

Job Sub Function:

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All Job Posting Locations:

Danvers, Massachusetts, United States of America

Job Description:

Johnson & Johnson is currently seeking a Production Engineering Co-op to join the Production Engineering team in Danvers, MA

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 Med Tech, 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  .

Program Dates:

January 11, 2027 - June 25, 2027

Role Requirements:

The Production Engineering Co-op will support the design, development, improvement, and validation of manufacturing processes, tooling, and fixtures. The role will contribute to daily production needs, defect reduction, productivity improvements, and product quality while working with global, cross-functional Operations, Product Development, and Quality Assurance teams.

  • Support global process improvement, production-floor support, and production-transfer activities through recurring meeting coordination and attendance.
  • Work in cross-functional teams that span global operations.
  • Use Lean and Six Sigma tools to analyze process trends, communicate issues using a data-driven approach, and identify opportunities to improve process performance and yield.
  • Support commercial production of new products, product changes, and enhancements in coordination with Operations, Product Development, and Quality Assurance.
  • Support and enforce company goals, policies, and procedures, including Good Manufacturing Practices, Good Documentation Practices, FDA Quality System Regulation requirements, and applicable ISO standards.
  • Assist with developing and maintaining process documentation, including assembly and test procedures, routers, travelers, bills of materials, process flows, and process FMEAs.
  • Help execute process validations, including preparation of validation plans, protocols, and reports.
  • Qualify and optimize processes and tooling through IQ/OQ/PQ, Gage R&R studies, process capability studies, and design of experiments.
  • Participate in failure investigations and in the development and implementation of action plans addressing internal corrective actions and audit findings.
  • Maintain accurate documentation of concepts, designs, and processes while staying current on medical, technical, and biomedical developments related to Abiomed products.
  • Work with product development staff to ensure products under development are designed appropriately for manufacturing, testing, and inspection.
Qualifications:
  • Junior, Senior, or graduate student pursuing an engineering degree.
  • Prior work experience is desired; medical device experience is preferred.
  • Knowledge of Lean, Six Sigma, Kaizen, and continuous improvement methods;
    Green Belt certification is preferred.
  • Ability to communicate ideas and information clearly and effectively, both verbally and in writing.
  • Ability to prioritize work and complete tasks in a timely manner with limited direct supervision.
  • Proficiency in Microsoft Office; working knowledge of SAP is desired.
  • Applicants must be authorized to work for any employer in the United States. Employment sponsorship is not available now or in the future.
  • 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,…
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