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Production Engineering Co-op

Full-time

Johnson & Johnson

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech 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 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:

Career Programs

Job Sub Function:

Non-LDP Intern/Co-Op

Job Category:

Career Program

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 & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech 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 more at 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 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.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin disability protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation external applicants please contact us via . Internal employees contact AskGS to be directed to your accommodation resource.

#LI-Onsite

Required Skills:

Preferred Skills:

The anticipated base pay range for this position is :

Additional Description for Pay Transparency:

Required Experience:

IC

Vacancy posted 6 days ago
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