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Supplier Excellence Lead (Medical Manufacturing)

80 000 - 110 000$
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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Описание вакансии

Текст:
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TL;DR
Supplier Excellence Lead (Medical Manufacturing): Delivering material and component cost reductions, supply resilience, and margin improvement through technical analysis, specification optimization, alternate sourcing, and cross-functional execution with an accent on value engineering, supplier qualification, and regulated manufacturing. Focus on leading technical changes, validating savings opportunities, mitigating supply risks, and transferring completed initiatives into operations.

Location: Aibonito, Puerto Rico; applicants must be authorized to work for a U.S. employer

Salary: $80,000–$110,000 annually

Company

hirify.global develops healthcare products and solutions with a mission to save and sustain lives.

What you will do

  • Identify and evaluate total cost optimization opportunities across materials, components, and manufacturing processes.
  • Perform should-cost, clean-sheet, teardown, cost-driver, and benchmarking analyses.
  • Lead cross-functional technical teams through project planning, technical changes, trials, testing, validation, and implementation.
  • Partner with Procurement, Quality, R&D, Operations, Strategy, Finance, and suppliers on cost and supply initiatives.
  • Support alternate sourcing, dual qualification, supplier readiness, risk mitigation, and capacity assessments.
  • Track projects from opportunity assessment and business case development through execution, savings handover, and governance reporting.

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.
  • Experience leading cross-functional projects end to end using structured project management methods.
  • Working knowledge of GMP, change control, deviation/CAPA concepts, and validation and qualification principles.
  • Strong analytical, communication, and cross-functional influence skills.
  • Must be authorized to work for a U.S. employer; visa sponsorship or transfer of employment-visa sponsorship is not available. Travel is required approximately 50% of the time.

Nice to have

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

Culture & Benefits

  • Collaborative, cross-functional manufacturing environment focused on quality, innovation, and continuous improvement.
  • Opportunities for professional development and continuing education.
  • Eligible employee benefits include medical and dental coverage, life and disability insurance, retirement savings with company matching, educational assistance, and paid time off.
  • Additional benefits may include employee stock purchase options, flexible spending accounts, parental leave, commuting support, childcare benefits, and employee assistance programs.

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