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8 дней назад

Quality Control Technician (Medical Devices)

Формат работы
onsite
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
UK
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
Quality Control Technician (Medical Devices): Performing in-process testing and inspections of medical devices in a fast-paced manufacturing environment with an accent on compliance, accurate documentation, and safety. Focus on operating inspection equipment, reporting non-conformances, and resolving quality issues with production and engineering teams.

Location: Cardiff, United Kingdom; on-site shift role. Weekly rotation between 6:00–14:00 and 14:00–22:00.

Company

hirify.global’s Cytiva operating company develops solutions for life sciences, diagnostics, biotechnology, and human health.

What you will do

  • Perform in-process testing and inspections of medical devices using testing equipment and work instructions.
  • Meet hourly targets and follow safety requirements.
  • Document and report test results and non-conformances accurately and promptly.
  • Collaborate with production and engineering teams to identify and resolve quality issues.
  • Maintain a clean, organised, safe, and efficient work area.

Requirements

  • At least one year of experience in a manufacturing facility or similar environment.
  • Ability to work under pressure with minimal supervision and use personal initiative.
  • Strong attention to detail and focus on safety, quality, and delivery.
  • Availability for the specified on-site rotating shift pattern.

Nice to have

  • Experience using measurement tools and inspection equipment.
  • Experience in quality control, ISO 9001, ISO 13485, or pharmaceutical-regulated manufacturing.
  • Ability to make reasoned and objective decisions.

Culture & Benefits

  • Work in a life sciences and medical technology environment focused on improving human health.
  • Use hirify.global’s continuous improvement system to support operational and quality improvements.
  • Collaborate with production, engineering, and quality control colleagues.
  • Contribute to solutions supporting biological research, vaccines, medicines, and cell and gene therapies.

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