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28 дней назад

Manufacturing Lead - Diurno 4 x 3 M - S (Medical Devices)

Формат работы
onsite
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
CR
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 Lead - Diurno 4 x 3 M - S (Medical Devices): Managing medical-device manufacturing activities and production operators in Alajuela with an accent on process certification, quality inspection, documentation, and line balancing. Focus on scheduling and coaching operators, maintaining process coverage, resolving equipment and process issues, and meeting productivity and quality goals.

Location: Alajuela, Costa Rica. Onsite work schedule: Diurno 4x3, Wednesday to Saturday, 6:00 a.m. – 6:00 p.m. Occasional travel may be required.

Company

hirify.global operates in medical-device manufacturing.

What you will do

  • Manage production associates and create daily job assignment schedules.
  • Coordinate and perform hands-on manufacturing activities according to work instructions, operating procedures, and approved documentation.
  • Maintain line balance, productivity, quality, and primary/back-up coverage for critical process steps.
  • Train and coach operators, support certification activities, and mentor less experienced personnel.
  • Perform inspections, measurements, data collection, lot closure, and manufacturing documentation.
  • Communicate process, equipment, Servoy, IT, and Epicor issues to supervisors and support groups.

Requirements

  • High school degree and 6–7 years of related experience.
  • Ability to read, write, and understand English.
  • Experience interpreting engineering drawings, technical documentation, machine performance results, safety rules, and operating procedures.
  • Ability to use measuring devices, optical comparators, video systems, magnification systems, and inspection equipment.
  • Basic PC, email, word processing, spreadsheet, and graphics skills.
  • Ability to work varying shifts and overtime, follow safety and production procedures, and meet clean-room and visual-work standards.

Nice to have

  • Knowledge of Servoy and the C-Pro training certification module.
  • Experience with medical-device process controls, QSR, and ISO requirements.

Culture & Benefits

  • Indoor, well-lighted, heated or air-conditioned work environment with adequate ventilation.
  • Clean-room work requiring special garments and compliance with health, safety, and environmental procedures.
  • Light physical activity with occasional lifting or carrying and moderate noise exposure.
  • Reasonable accommodations may be provided for individuals with disabilities.

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