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7 часов назад

Principal Manufacturing Engineer (MES)

123 200 - 184 800$
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Principal Manufacturing Engineer (MES): Designing, implementing, and optimizing Manufacturing Execution Systems for regulated medical-device manufacturing with an accent on MES architecture, ERP and quality-system integration, validation, and regulatory traceability. Focus on leading cross-functional digital manufacturing projects, solving compliance and process-control challenges, and improving system performance through DMAIC and data analysis.

Location: Lafayette, Colorado, United States

Salary: $123,200–$184,800 per year, plus eligibility for the hirify.global Incentive Plan.

Company

hirify.global is a global healthcare technology company developing medical technologies across more than 150 countries.

What you will do

  • Lead the implementation, enhancement, support, and optimization of Manufacturing Execution Systems.
  • Design MES architecture, workflows, configurations, work instructions, process maps, and technical documentation.
  • Integrate MES with ERP, quality, manufacturing, and other production systems.
  • Partner with Operations, Manufacturing, Quality, Engineering, and IT teams to deliver digital manufacturing solutions.
  • Drive continuous improvement through manufacturing-process analysis, system metrics, operational data, and DMAIC.
  • Lead validation activities, change control, audits, user training, and complex cross-functional manufacturing-systems projects.

Requirements

  • Bachelor’s degree in Engineering, Manufacturing Engineering, Industrial Engineering, Computer Science, Information Systems, or a related technical field.
  • 7+ years of experience in manufacturing engineering, manufacturing systems, digital manufacturing, MES, or related technical disciplines.
  • Experience implementing, supporting, or optimizing MES in a regulated manufacturing environment.
  • Experience integrating ERP, quality, and manufacturing systems.
  • Knowledge of manufacturing process controls, quality systems, GMP, and 21 CFR Part 11.
  • Experience with software validation and qualification activities in regulated industries.

Nice to have

  • Advanced degree in Engineering, Manufacturing, Operations, or a related field.
  • Medical device, pharmaceutical, biotech, or other regulated-industry experience.
  • Experience with Tulip, Camstar, Opcenter, FactoryTalk, PAS-X, electronic batch records, or electronic device history records.
  • Lean Manufacturing, Six Sigma, PMP, digital transformation, Industry 4.0, smart factory, dashboards, or manufacturing analytics experience.

Culture & Benefits

  • Full-time regular employment with health, dental, vision, life, disability, and retirement benefits.
  • 401(k) plan with employer contribution and match, paid time off, and paid holidays.
  • Health Savings Account, Flexible Spending Account, dependent-care spending account, and tuition assistance.
  • Incentive plans, Employee Stock Purchase Plan, Employee Assistance Program, and well-being resources.
  • U.S. work authorization sponsorship is offered for Principal-level roles and above.

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