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Technical Lead - Value Engineering (Medtech)

80 000 - 100 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Текст:
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TL;DR
Technical Lead - Value Engineering (Medtech) (Technical Cost Out/value engineering): Delivering material, component, and process cost reductions across regulated manufacturing sites with an accent on should-cost analysis, specification optimization, alternate sourcing, and supply resilience. Focus on leading technical changes, validating substitutions, coordinating suppliers and cross-functional teams, and implementing savings while maintaining product performance, compliance, and continuity.

Location: Aibonito, Puerto Rico

Salary: $80,000–$100,000 annually

Company

hirify.global develops and manufactures healthcare products focused on its mission to save and sustain lives.

What you will do

  • Identify and evaluate material, component, and process cost-optimization opportunities across manufacturing sites.
  • Perform should-cost, clean-sheet, teardown, benchmarking, and value-engineering analyses.
  • Lead cross-functional technical projects involving specification changes, material substitutions, sample builds, trials, testing, validation, and implementation.
  • Collaborate with Procurement, R&D, Quality, Operations, Strategy, Finance, and suppliers on sourcing, qualification, resilience, and capacity initiatives.
  • Track opportunities from assessment and business case development through execution, savings handover, documentation, and governance.
  • Escalate quality, service, regulatory, cost, and timeline risks while documenting best practices.

Requirements

  • 5–8+ years of experience and a bachelor’s degree in Mechanical, Materials, Plastics, Chemicals, Packaging, Manufacturing Engineering, or a related field.
  • Proven delivery of multi-million-dollar value-engineering savings and end-to-end cross-functional projects.
  • Working knowledge of GMP, change control, deviation/CAPA concepts, and validation or qualification principles.
  • Strong analytical, communication, and cross-functional influence skills.
  • Travel required at 10–20%.
  • Must be authorized to work for an employer in the United States; visa sponsorship is not available.

Nice to have

  • Experience with alternate sourcing, supplier qualification, APQP/PPAP, regulated manufacturing, insourcing, technical transfers, and procurement leadership.
  • Experience in value engineering, design for manufacturability, cost modelling, should-costing, or clean-sheet methodologies.
  • Lean or Six Sigma certification.

Culture & Benefits

  • Collaborative, cross-functional manufacturing environment focused on quality and continuous improvement.
  • Opportunities for professional development and continuous education.
  • Eligible employee benefits may include medical and dental coverage, insurance, retirement programs, paid time off, parental leave, educational assistance, and employee support programs.
  • Overtime may be required.

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