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8 часов назад

Fixed Term Manufacturing Associate I (mRNA Manufacturing)

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
Fixed Term Manufacturing Associate I (mRNA Manufacturing) (mRNA vaccine production): Operating advanced manufacturing systems for mRNA vaccines with an accent on cGMP compliance, production documentation, equipment operation, and quality assurance. Focus on troubleshooting equipment and digital systems, investigating deviations through root cause analysis and CAPA, performing basic maintenance, and supporting continuous improvement in a 24/7 manufacturing environment.

Location: Oxford, England, United Kingdom. Onsite manufacturing role with a fixed 24/7 2-2-3 shift pattern and 12-hour shifts.

Compensation: Competitive pay and benefits; no exact salary stated.

Company

hirify.global develops mRNA technology and medicines, including vaccines, through advanced scientific and digital manufacturing platforms.

What you will do

  • Operate equipment used in mRNA vaccine production according to cGMP requirements, SOPs, and approved manufacturing documentation.
  • Execute production activities while maintaining quality, compliance, health, safety, housekeeping, and inspection-readiness standards.
  • Partner with Quality Assurance to complete production records supporting the timely disposition of commercial batches.
  • Investigate manufacturing deviations and incidents using root cause analysis, and support corrective and preventive actions.
  • Troubleshoot routine equipment, process, and digital system issues; perform basic maintenance including lubrication, mechanical checks, and filter changes.
  • Support operational KPIs, cross-functional projects, continuous improvement initiatives, and adoption of new mRNA manufacturing technologies and digital 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.
  • Ability to collaborate with peers, leadership, Quality Assurance, and cross-functional support groups.
  • Strong written and oral communication, organizational skills, attention to detail, and ability to manage multiple tasks with minimal supervision.
  • Ability to support off-hours work and overtime according to business needs.

Nice to have

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

Culture & Benefits

  • Technology-driven manufacturing environment focused on scientific thinking, operational excellence, continuous learning, and innovation.
  • Healthcare and voluntary benefit programs.
  • Fitness, mindfulness, and mental health support.
  • Family-building benefits, including fertility, adoption, and surrogacy support.
  • Paid vacation, bank holidays, volunteer days, sabbatical, global recharge days, and discretionary year-end shutdown.
  • Savings and investment programs, plus location-specific benefits.

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