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Manufacturing Engineering Manager (MedTech)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior/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
Manufacturing Engineering Manager (MedTech): Leading manufacturing engineering teams and improving regulated medical-device production through process robustness, yield improvement, equipment reliability, validation, and technical investigations with an accent on GMP/ISO compliance and operational performance. Focus on developing engineers, prioritizing complex engineering programs, executing FAT/IQ/OQ/PQ validation, and driving root-cause analysis and continuous improvement.

Location: Añasco, Puerto Rico, United States; fully onsite. Requires up to 10% travel.

Company

Johnson & Johnson MedTech develops innovative, less invasive, and personalized healthcare and vision treatments.

What you will do

  • Lead, coach, and develop the manufacturing engineering team while establishing priorities, accountability, and leadership routines.
  • Set engineering standards and governance for manufacturing areas, including line-side support, escalation, and structured problem solving.
  • Drive yield, UPPH, uptime, OEE, process reliability, and productivity improvements through trend analysis and risk-based prioritization.
  • Lead manufacturing engineering programs and projects, ensuring safety, regulatory compliance, financial discipline, and operational delivery.
  • Direct root-cause analysis, non-conformance investigations, corrective and preventive actions, process characterization, and equipment support.
  • Develop resource-planning and project-prioritization systems and partner with Operations, Quality, Maintenance, Automation, Facilities, Supply Chain, Finance, Human Resources, and global engineering.

Requirements

  • Bachelor’s degree in Engineering is required.
  • At least 8 years of relevant experience in manufacturing engineering, maintenance manufacturing, process development, R&D, automation, or regulated manufacturing operations is preferred.
  • People leadership or demonstrated technical/team leadership experience is required.
  • Experience with GMP/ISO requirements, validation lifecycle, FAT, IQ, OQ, PQ, process characterization, and technical investigations is preferred.
  • Strong communication, cross-functional collaboration, decision-making, coaching, and stakeholder management skills are required.
  • Medical device or pharmaceutical industry experience, project and financial management, resource planning, optical inspection, automated equipment, and process optimization experience are preferred.

Culture & Benefits

  • Work in a regulated GMP/ISO manufacturing environment with a focus on technical excellence and continuous improvement.
  • Support is provided for physical, mental, emotional, and financial health programs.
  • Employment requires proof of COVID-19 vaccination or an approved accommodation before starting.
  • Inclusive and equal-opportunity workplace.

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