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6 дней назад

Senior Supplier Engineer (MedTech)

109 000 - 174 800$
Формат работы
onsite
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
Senior Supplier Engineer (MedTech): Designing, developing, and validating manufacturing solutions for direct-material components and assemblies in medical-device robotics and digital solutions with an accent on supplier process development, manufacturing scale-up, and regulatory compliance. Focus on resolving complex manufacturing challenges, driving supplier quality and continuous improvement, and validating robust production processes.

Location: Santa Clara, California, United States of America; fully on-site. Up to 25% domestic and international travel is required.

Salary: $109,000–$174,800 base pay per year.

Company

Johnson & Johnson MedTech develops healthcare and medical-device solutions, including next-generation robotic and digital technologies.

What you will do

  • Design, develop, characterize, and validate supplier manufacturing processes for direct-material components and subassemblies.
  • Support new product development and sustaining production within the Robotics and Digital Solutions franchise.
  • Collaborate with Manufacturing Engineering, R&D, Sourcing, Quality, Supply Chain, Marketing, and Finance teams.
  • Drive supplier performance improvements using project management, Six Sigma, Lean, SPC, negotiation, and root cause analysis.
  • Manage supplier requirements for tooling, manufacturing, inspections, corrective actions, and preventive actions.
  • Support cost reduction, capacity and efficiency improvements, and supply-chain optimization.

Requirements

  • BS degree in Engineering or equivalent.
  • At least five years of meaningful experience in a regulated industry; medical-device experience is preferred.
  • Experience with manufacturing process characterization, development, and validation.
  • Knowledge of engineering drawing interpretation and GD&T.
  • Knowledge of manufacturing technologies such as plastic injection molding, extrusion, machining, SMT, PCB, electrical components, or assembly.
  • Strong knowledge of 21 CFR Part 820 and ISO 13485, plus regulatory requirements for designing, manufacturing, and releasing medical devices.

Nice to have

  • Project management experience.
  • Knowledge of SPC, capability analysis, FMEA, DFM/A, supplier qualification and selection, and supplier process improvement.
  • Experience with root cause analysis and regulated medical-device manufacturing.

Culture & Benefits

  • Inclusive work environment guided by the company’s Credo.
  • Eligibility for a consolidated retirement plan and 401(k) savings plan.
  • Participation in a long-term incentive program.
  • Vacation, sick time, holidays, personal and family time, parental leave, bereavement leave, caregiver leave, volunteer leave, and military spouse time off.

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