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2 дня назад

Microbiologist II - Non-Sterile (Microbiology)

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
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
Microbiologist II - Non-Sterile (Microbiology): Performing microbiological testing, quality control, and aseptic production of BSL-1 and BSL-2 microbial stocks with an accent on routine and complex sample testing, result interpretation, and laboratory compliance. Focus on investigating unexpected results, maintaining regulated microorganisms and equipment, and supporting pharmaceutical and biochemical QC activities.

Location: Houston, Texas, United States; onsite laboratory role

Company

hirify.global provides microbiological testing, calibration, and scientific compliance solutions for pharmaceutical, compounding, healthcare, and clinical research organizations.

What you will do

  • Perform routine and complex microbiological testing on samples and interpret results to determine pass or fail.
  • Conduct manufacturing and quality control testing for in-house media production.
  • Produce and handle BSL-1 and BSL-2 microbial stocks using aseptic techniques.
  • Record, report, and investigate unexpected test results with appropriate supervision.
  • Maintain laboratory equipment, perform basic troubleshooting, and report calibration or repair issues.
  • Maintain accurate documentation, support compliance and safety audits, and provide backup support across laboratory workstations.

Requirements

  • Bachelor’s degree in microbiology or a related science field, including at least 12 semester hours of hands-on microbiology and/or chemistry laboratory courses.
  • At least 3 years of pharmaceutical or biochemical QC laboratory experience in a microbiology setting, or an MS degree.
  • Experience with microbiological functions such as microbial enumeration, growth promotion testing, environmental monitoring, microbial identification, gram staining, pipetting, or method suitability.
  • Working knowledge of microbiology principles, methods, laboratory problem-solving, and technical documentation.
  • Ability to work independently, manage multiple tasks, follow SOPs and safety rules, and maintain accurate testing.
  • Intermediate proficiency with Microsoft Office, Word, Excel, Outlook, and PowerPoint.

Nice to have

  • Pharmaceutical, biotech, clinical laboratory, or QC experience.
  • At least 2 years of GMP or cGMP experience.
  • Experience with virology, fibrology, and SOP creation and implementation.

Culture & Benefits

  • Full-time schedule with either Tuesday–Saturday first shift, 7:00 AM–4:00 PM, or Monday–Friday second shift, 11:00 AM–8:00 PM.
  • Cross-technology education covering laboratory functions, microorganisms, instruments, troubleshooting, and microbiology taxonomy.
  • Work in a regulated laboratory environment following ISO 17025, BSLT-2 cGMP, cGLP, A2LA, and quality control requirements.
  • Emphasis on teamwork, detail orientation, independent work, and contribution to laboratory and customer outcomes.

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