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12 дней назад

Quality Control Associate, Microbiology

Формат работы
hybrid
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
Spain
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 Associate, Microbiology (Biotech/mRNA): Performing cGMP microbiology testing for the release and stability of innovative mRNA medicines with an accent on endotoxin, sterility, environmental monitoring, and data integrity. Focus on troubleshooting assay methods, supporting OOS investigations and CAPA activities, and maintaining inspection-ready laboratory documentation.

Location: Madrid, Spain; hybrid 70/30 work model with 70% in-office collaboration.

Company

hirify.global develops mRNA medicines and operates an analytical excellence centre in Madrid that supports its global manufacturing network and mRNA portfolio.

What you will do

  • Perform cGMP Quality Control Microbiology testing for release and stability programs, including endotoxin, sterility, environmental monitoring, and microbial sequencing.
  • Support method qualification, method acquisition, stability programs, and testing of drug substances and drug products.
  • Enter and trend data in electronic systems, including Electronic Assay Forms and LabVantage LIMS.
  • Perform laboratory support activities such as reagent preparation, sample management, growth promotion, equipment maintenance, inventory control, and contract laboratory sample coordination.
  • Troubleshoot microbiological assays and equipment, and support investigations involving OOS and other non-conforming results.
  • Participate in deviations, CAPA activities, GMP documentation, training, and continuous improvement while maintaining a safe laboratory environment.

Requirements

  • Technical qualification or degree in Biology, Biochemistry, or another relevant scientific discipline.
  • At least 2 years of relevant experience; quality control laboratory experience in a pharmaceutical company is preferred.
  • Hands-on experience with growth promotion, endotoxin testing, and sterility testing in QC microbiology laboratories.
  • Working knowledge of current FDA, EU, and ICH guidelines and regulations is preferred.
  • Ability to collaborate in a cross-functional matrix environment and prioritize multiple tasks in a fast-paced setting.
  • Working proficiency in English is required.

Culture & Benefits

  • 70/30 in-office work model focused on collaboration, innovation, teamwork, and direct mentorship.
  • Healthcare and voluntary benefit programs.
  • Fitness, mindfulness, and mental health support.
  • Family-building benefits, including fertility, adoption, and surrogacy support.
  • Paid time off, bank holidays, volunteer days, sabbatical, global recharge days, and year-end shutdown.
  • Savings and investment programs plus location-specific benefits.

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