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Engineering Manufacturing Maintenance Supervisor (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
Engineering Manufacturing Maintenance Supervisor (MedTech): Supervising maintenance and repair of production equipment in a medical device manufacturing plant with an accent on equipment reliability, preventive and predictive maintenance, GMP compliance, and technician development. Focus on coordinating repairs and upgrades, maintaining equipment performance, managing spare parts and contractors, and meeting safety and regulatory requirements.

Location: Anasco, Puerto Rico, United States of America

Company

Johnson & Johnson MedTech develops healthcare and vision treatment products that combine medical science and technology.

What you will do

  • Supervise maintenance technicians and coordinate the repair, operation, overhaul, and upgrade of manufacturing equipment.
  • Maintain preventive, corrective, and predictive maintenance programs while monitoring equipment performance and downtime.
  • Coordinate contracted services, spare parts, tools, validation activities, and maintenance priorities with production operations.
  • Track team performance, set goals, provide feedback, and develop training programs to improve productivity and service levels.
  • Collaborate with Quality Assurance, Operations, EHS, maintenance planning, and spare-parts teams.
  • Conduct production-area audits and ensure compliance with GMP, safety, environmental, corporate, and regulatory requirements.

Requirements

  • Bachelor’s degree in Engineering.
  • At least 2 years of experience in a manufacturing maintenance environment.
  • Ability to read, speak, and write both Spanish and English.
  • Demonstrated leadership experience as a lead or supervisor, including delegation, follow-up, performance management, and conflict resolution.
  • Computer literacy in email, word processing, and spreadsheets, with strong attention to detail and deadline management.
  • Knowledge of FDA regulations is preferred; medical device industry experience is preferred.

Culture & Benefits

  • Full-time employment in a manufacturing environment.
  • Commitment to an inclusive workplace based on individual respect, diversity, and dignity.
  • Focus on safety, teamwork, environmental responsibility, and Credo-based collaboration.
  • Inclusive interview accommodations are available for candidates with disabilities.

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