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5 дней назад

Mgr Process Engineering (MedTech)

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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Описание вакансии

Текст:
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TL;DR
Mgr Process Engineering (MedTech): Leading manufacturing process engineering and production operations for optical tooling and mold servicing with an accent on safety, quality, regulatory compliance, and output improvement. Focus on supervising production staff, resolving operational and maintenance problems, coordinating cross-functional teams, and maintaining audit readiness across rotating 12-hour shifts.

Location: Jacksonville, Florida, United States of America; onsite role with regular rotating 12-hour shifts from 6 p.m. to 6 a.m., including weekends.

Company

Johnson & Johnson MedTech develops healthcare and vision solutions that combine biology, technology, and medical innovation.

What you will do

  • Lead and supervise manufacturing staff in Optical Tooling and Mold Servicing operations.
  • Manage production performance across safety, quality, cost, schedule, and regulatory compliance.
  • Coordinate the resolution of operational, manufacturing, maintenance, and facilities issues.
  • Conduct Gemba walks and maintain audit and compliance readiness.
  • Collaborate with Safety, Quality, Manufacturing, Planning, Engineering, and Facilities teams.
  • Manage performance reviews, training curricula, schedules, and product-line assignments.

Requirements

  • Vocational or technical certificate, or equivalent experience.
  • 2–4 years of manufacturing experience and at least 2 years of frontline supervisory experience.
  • Ability to lead in an empowered team environment and manage production personnel.
  • Strong written and oral communication skills.
  • Proficiency with Outlook, Excel, Word, and PowerPoint.
  • Ability to work regular rotating 12-hour shifts from 6 p.m. to 6 a.m., including weekends.

Nice to have

  • Bachelor’s degree or equivalent experience.
  • 6+ years of relevant supply chain experience and 4+ years of supervisory experience.
  • Experience with ISO, FDA, and GMP-regulated manufacturing environments.
  • Six Sigma or Lean Manufacturing certification.
  • Knowledge of timekeeping processes.

Culture & Benefits

  • Inclusive work environment focused on diversity, dignity, and employee development.
  • Cross-functional collaboration across manufacturing, engineering, quality, safety, planning, and facilities.
  • Work in a healthcare and vision-focused MedTech environment.

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