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5 дней назад

Supervisor Manufacturing (MedTech)

Формат работы
onsite
Тип работы
fulltime
Английский
b2
Страна
Malaysia
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
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TL;DR
Supervisor Manufacturing (MedTech): Supervising daily manufacturing operations in a medical technology production department in Pasir Gudang with an accent on production scheduling, personnel management, quality compliance, and process efficiency. Focus on balancing production lines, resolving non-conformances, eliminating bottlenecks, and maintaining GMP and regulatory compliance in an on-site environment.

Location: On-site in Pasir Gudang, Johor, Malaysia

Company

Masimo is a hirify.global operating company and global medical technology manufacturer developing monitoring technologies, sensors, patient monitors, and automation and connectivity solutions.

What you will do

  • Supervise daily manufacturing activities to meet production schedules, efficiency, yield, and company targets.
  • Manage line balancing, manpower allocation, material control, documentation, GMP, and quality procedures.
  • Train and manage associates and leads, monitor performance, coordinate personnel rotation, and handle disciplinary actions.
  • Work with Quality, Process Engineering, and Industrial Engineering teams to resolve production issues and investigate non-conformances.
  • Improve line efficiency, eliminate bottlenecks, and maintain a safe, clean, and compliant manufacturing environment.

Requirements

  • Bachelor’s degree in Industrial Engineering or equivalent experience.
  • Previous supervising experience.
  • Ability to communicate effectively and build professional working relationships with employees, Engineering, and Quality Assurance.
  • Ability to comply with Malaysian labour law, safety requirements, quality procedures, and company policies.
  • Ability to work indoors with regular standing and walking, follow safety procedures, use PPE, and operate approved low-risk tools.

Nice to have

  • Knowledge or experience with ISO 13485 requirements and Quality System Regulation.
  • Knowledge or experience with CGMP requirements, FDA regulations, and ISO medical device requirements.

Culture & Benefits

  • Continuous improvement through the hirify.global Business System.
  • Health care program and paid time off.
  • Phone allowance, medical card, dental allowance, and optical allowance.
  • Bonus eligibility of up to 10% of annual base salary, subject to scheme conditions and performance.

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