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5 дней назад

(Fixed Term) Manufacturing Associate I (mRNA)

Формат работы
onsite
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
UK/US
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): Operating equipment and executing GMP-compliant manufacturing operations for mRNA vaccine production with an accent on production documentation, quality compliance, and digital manufacturing systems. Focus on troubleshooting equipment and process issues, supporting deviation investigations and CAPA, and maintaining operational performance in a 12-hour 2-2-3 shift schedule.

Location: Oxford, England, United Kingdom. In-person manufacturing role with a 24/7 fixed 12-hour shift pattern on a 2-2-3 schedule.

Salary: Competitive compensation; exact amount not specified.

Company

hirify.global develops mRNA-based medicines and vaccines through advances in mRNA science, delivery technology, and manufacturing.

What you will do

  • Operate manufacturing equipment for mRNA vaccine production under cGMP, SOPs, and approved manufacturing documentation.
  • Maintain safe, compliant, inspection-ready manufacturing areas, including gowning, housekeeping, and environmental health and safety procedures.
  • Complete production documentation with Quality Assurance to support timely commercial batch disposition.
  • Investigate manufacturing deviations and incidents using root cause analysis and support CAPA implementation.
  • Troubleshoot routine equipment, manufacturing process, and digital system issues; perform basic equipment maintenance.
  • Support operational KPIs, continuous improvement projects, cross-functional collaboration, and off-hours or overtime work when required.

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 verbal communication, organization, attention to detail, and ability to work with minimal supervision.
  • Flexibility to work 12-hour shifts in a 2-2-3 schedule, including off-hours and overtime when needed.

Nice to have

  • Experience with filtration and chromatography.
  • Experience with cold chain management.
  • Experience using digital and Generative AI-enabled manufacturing technologies.

Culture & Benefits

  • Technology-driven manufacturing environment focused on scientific thinking, operational excellence, learning, and continuous improvement.
  • Healthcare and voluntary benefit programs.
  • Fitness, mindfulness, mental health, family-building, and location-specific support.
  • Paid vacation, bank holidays, volunteer days, sabbatical, global recharge days, and year-end shutdown.
  • Savings and investment programs.

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