J

Jabil

Designs and builds electronics for other brands

Manufacturing Engineer 3 - Heading Department

Manufacturing EngineeringConfirmed live in the last 24 hours
Full-timeMonument, CO, USA

About the Job

Requirements

  • A Bachelor's degree in Mechanical, Manufacturing, Industrial Engineering, or a related technical discipline is preferred.
  • At least five years of related manufacturing engineering experience, or an equivalent combination of education and experience.
  • Experience with precision forming, tooling development, or high-volume manufacturing is preferred; a background in manual or automated production equipment is strongly preferred.
  • Experience working within a regulated medical device quality system is preferred, including familiarity with documentation control, product and material traceability, validation, change control, and good documentation practices.
  • Lean Six Sigma experience and demonstrated use of structured continuous improvement methods are preferred; Green Belt certification or equivalent practical experience is a plus.
  • Strong written, verbal, interpersonal, and presentation skills, including the ability to communicate technical information, project status, recommendations, and results to operators, engineers, leadership, customers, and cross-functional teams.
  • Strong computer skills, including Microsoft Office, Minitab, and databases.
  • Strong organizational and project management skills.
  • Advanced troubleshooting skills for forming processes, tooling, equipment set-up, dimensional variation, and related manufacturing issues.
  • Understand and comply with applicable medical device regulations and quality-system requirements, including Quality System Regulation (QSR), Standard Operating Procedures (SOPs), approved Work Instructions, documentation controls, and traceability requirements. Perform work in accordance with current approved procedures and complete documentation accurately and contemporaneously.
  • Follow applicable laws and policies and maintain professionalism, ethics, and compliance.
  • Support and operate in a proactive safety environment.
  • Applicants must be legally authorized to work in the United States without current or future sponsorship by Jabil.

Responsibilities

  • Provide technical leadership for continuous improvement of forming and related manufacturing operations by evaluating and implementing technologies, Lean Six Sigma methods, and process improvements that enhance quality, cost, capacity, and capability.
  • Support manufacturing in meeting quality-system, documentation, product traceability, capacity, product availability, and cost requirements within a regulated medical device environment.
  • Provide technical support for header and cam-machine operations, including equipment troubleshooting, upgrades, set-ups, process development, parameter optimization, and continuous improvement.
  • Design and develop die and punch-form tooling and select appropriate materials, equipment, automation, workholding, and inspection methods to support robust, repeatable, and cost-effective manufacturing processes.
  • Perform dimensional tolerance stack-up analyses to evaluate design requirements, process capability, tooling interactions, and potential sources of variation.
  • Perform assignments that continue the development of professional work knowledge and abilities, applying standard engineering techniques, procedures, and criteria to related engineering tasks, project management, statistical analysis, data presentation, and technical writing.
  • Lead product and manufacturing process changes, new product development, and process transfers to improve efficiency, quality, capacity, and cost; recommend design changes that improve manufacturability and assembly.
  • Use PTC Creo and Windchill to support product, tooling, and process documentation; comparable CAD software such as SolidWorks is acceptable, and training on PTC Creo and Windchill can be completed on the job.
  • Collaborate with customers, vendors, and cross-functional teams on design reviews and technical recommendations.
  • Plan, author, execute, and report on proof-of-concept experiments, design of experiments, capability studies, equipment acceptance and qualification activities, and process validations, including SAT, FAT, IQ, OQ, and PQ documentation, for assigned products, equipment, and manufacturing processes.
  • Author, maintain, and review clear, accurate, and compliant engineering documentation, including validation plans, protocols, reports, standard operating procedures, work instructions, and operations and maintenance documentation.
  • Ensure assigned projects comply with applicable regulatory requirements and support company safety and quality programs and initiatives.
  • Perform other duties and responsibilities as assigned.

Desired Qualifications

  • Experience with precision forming, tooling development, or high-volume manufacturing; a background in manual or automated production equipment is strongly preferred.
  • Experience working within a regulated medical device quality system, including familiarity with documentation control, product and material traceability, validation, change control, and good documentation practices.
  • Lean Six Sigma experience and demonstrated use of structured continuous improvement methods; Green Belt certification or equivalent practical experience is a plus.

About the Company

Jabil

Designs and builds electronics for other brands

Jabil designs and manufactures electronics and other products for companies that sell them under their own brands, including makers of AI data center hardware, medical devices, cars, and defense systems. Customers bring a product idea or design, and Jabil handles the engineering, sources the parts, builds the product at scale, and manages the supply chain behind it. The work runs through a global network of factories, so one partner can build products for customers across many markets, from data center racks to medical equipment. Jabil earns revenue through manufacturing and engineering service contracts with these brands. The company was founded in 1966 and is based in St. Petersburg, Florida.

Company size
10,001+
Company stage
IPO
Headquarters
Saint Petersburg, Florida
Founded
1966

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