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7 часов назад

Manufacturing Associate I (mRNA Vaccines)

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
Manufacturing Associate I (mRNA Vaccines): Operating automated manufacturing equipment to produce commercial mRNA vaccine batches in a cGMP-regulated environment with an accent on safe production, accurate documentation, and operational compliance. Focus on troubleshooting equipment and digital systems, performing first-line maintenance, supporting deviation investigations and CAPA, and driving continuous improvement across manufacturing and quality functions.

Location: Oxford, England; in-person work in a highly automated manufacturing environment with a 24/7 fixed shift pattern.

Company

hirify.global develops mRNA technology and vaccines to transform how medicines are created and delivered.

What you will do

  • Operate manufacturing equipment and execute commercial vaccine production activities in accordance with cGMP, SOPs, manufacturing documentation, and health and safety requirements.
  • Maintain gowning, housekeeping, training records, and production documentation to support safe and compliant operations.
  • Work with Quality Assurance on batch documentation, investigations, root cause analysis, and corrective and preventive actions.
  • Troubleshoot routine equipment, process, and digital system issues and perform basic first-line maintenance using hand tools.
  • Monitor operational KPIs, escalate compliance and safety issues, and contribute to continuous improvement and technology adoption initiatives.
  • Collaborate with Manufacturing, Quality, Engineering, and other cross-functional teams, including support for emerging generative AI-enabled tools.

Requirements

  • At least 1 year of experience in a GMP manufacturing environment.
  • University degree specializing in pharmaceutical production technology or an equivalent qualification.
  • Experience preparing for audits or inspections and understanding health authority and regulatory guidelines.
  • Strong collaboration, written and oral communication, organizational, and digital skills.
  • Ability to maintain attention to detail while managing multiple tasks with minimal supervision.
  • Ability to work a 24/7 fixed 2-2-3 schedule with 12-hour shifts, including off-hours work and overtime when required.

Nice to have

  • Experience with filtration and chromatography.
  • Experience with cold chain management.

Culture & Benefits

  • Healthcare and voluntary benefit programs.
  • Fitness, mindfulness, and mental health support.
  • Family-building benefits, including fertility, adoption, and surrogacy support.
  • Paid time off including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown.
  • Savings and investment programs, plus location-specific benefits.
  • In-person collaboration supported by a 70/30 work model.

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