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9 часов назад

Assembly Team Leader (Medical Devices)

Формат работы
onsite
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
Ireland
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
Assembly Team Leader (Medical Devices): Leading evening-shift assembly and manufacturing operations in a regulated medical-device environment with an accent on safety, quality, GMP, productivity, and team capability. Focus on resource planning, Lean and 5S improvements, validated processes, production problem-solving, and collaboration with Engineering and Quality.

Location: Carrick-on-Shannon, County Leitrim, Ireland; evening-shift, on-site production role

Company

hirify.global operates in medical-device manufacturing and is part of the Freudenberg Group.

What you will do

  • Lead the day-to-day operation of the evening-shift production team, ensuring safety, quality, GMP, productivity, and waste targets are achieved.
  • Plan resources and manage the daily production schedule to meet manufacturing and customer requirements.
  • Train, coach, and develop Production Operators while ensuring consistent adherence to standard work.
  • Monitor production performance and KPIs, taking action to improve efficiency, quality, and output.
  • Drive Lean, 5S, problem-solving, continuous improvement, and waste-reduction initiatives.
  • Support process documentation, equipment issue resolution, New Product Introductions, change controls, product trials, validations, CAPA, audits, and investigations.

Requirements

  • Two to three years of experience leading or supervising a team in a manufacturing environment.
  • Ability to work an evening shift and take ownership of production activities during those hours.
  • Strong people leadership, coaching, motivation, communication, problem-solving, and cross-functional collaboration skills.
  • Good understanding of manufacturing productivity, efficiency, quality, and waste performance.
  • Experience in medical-device, pharmaceutical, or another regulated manufacturing environment is highly desirable.
  • Knowledge of ISO 13485 and FDA 21 CFR Part 820/QMSR, Lean manufacturing, 5S, and continuous improvement is advantageous.

Culture & Benefits

  • Focus on safety, quality, teamwork, accountability, diversity, and inclusion.
  • Opportunities for career progression as the manufacturing operation grows.

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