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21 день назад

Manufacturing Lead (Nocturno 4 x 3 M - S)

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 (Nocturno 4 x 3 M - S) (Medical Devices): Managing operators and coordinating hands-on production of medical devices in a Costa Rica manufacturing area with an accent on process certification, quality inspection, documentation, and line balancing. Focus on scheduling and coaching production associates, maintaining certified process coverage, resolving equipment and process issues, and meeting productivity and quality goals.

Location: Alajuela, Costa Rica; onsite night shift, Wednesday–Saturday, 6:00 p.m.–6:00 a.m.

Company

hirify.global manufactures medical devices in a regulated production environment.

What you will do

  • Manage Production Associates and coordinate daily assignments to meet productivity and quality goals.
  • Perform and support complex medical-device manufacturing processes, including testing, measurement, visual inspection, and lot closure.
  • Balance workstation assignments, maintain primary and backup process coverage, and coach operators toward additional certifications.
  • Resolve basic process, equipment, Servoy, IT, and Epicor issues with supervisors, maintenance, and support groups.
  • Complete manufacturing records, collect process data, and communicate production issues and updates to supervision and engineering.
  • Participate in process-improvement, safety, health, and environmental compliance activities.

Requirements

  • High school diploma and 6–7 years of related experience.
  • Ability to work onsite in Alajuela, Costa Rica, on a Wednesday–Saturday, 6:00 p.m.–6:00 a.m. schedule, with varying shifts and overtime as required.
  • Ability to read, write, and understand English.
  • Experience supervising or distributing work to production associates and communicating instructions effectively.
  • Ability to interpret engineering drawings, technical documentation, machine performance results, safety documents, and regulatory requirements such as QSR and ISO.
  • Ability to use computers, email, spreadsheets, measuring devices, optical comparators, video systems, and magnification equipment.

Culture & Benefits

  • Indoor, heated or air-conditioned manufacturing and clean-room environment with adequate ventilation.
  • Work involves occasional exposure to moving mechanical parts, fumes, chemicals, electrical shock risks, and UV light sources.
  • Special garments and annual visual-standard testing are required for clean-room work.
  • Occasional travel may be required.
  • Light physical activity, including lifting or carrying items, in a moderately noisy environment.

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