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37 минут назад

Microbiologist II - Non-Sterile

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/QC): Performing microbiological testing, in-house media manufacturing, and quality control for pharmaceutical and biochemical materials with an accent on BSL-1 and BSL-2 microbial stocks, aseptic production, and regulated laboratory compliance. Focus on interpreting and investigating test results, troubleshooting laboratory equipment, and maintaining accurate documentation under GMP, GLP, ISO 17025, and A2LA requirements.

Location: Houston, Texas, United States

Company

hirify.global presents Eagle as a laboratory services provider focused on sterility, bacterial endotoxin, microbial detection, beyond-use dating, and active ingredient potency testing.

What you will do

  • Perform routine and complex microbiological testing on samples, interpret results, and determine pass or fail outcomes.
  • Manufacture in-house media and produce BSL-1 and BSL-2 microbial stocks using aseptic techniques.
  • Handle BSL-2 microorganisms and investigate unexpected test results with supervision.
  • Maintain laboratory equipment, perform basic troubleshooting, and report calibration or repair issues.
  • Maintain accurate documentation and support compliance, quality, and laboratory safety audits.
  • Provide technical support across laboratory workstations and participate in cross-technology training.

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 testing such as enumeration, growth promotion, environmental monitoring, microbial identification, Gram staining, pipetting, or method suitability.
  • Knowledge of microbiology principles, laboratory problem-solving, SOP compliance, and safety procedures.
  • Ability to work independently with minimal supervision, manage multiple tasks, and communicate effectively.
  • Intermediate proficiency with Microsoft Office, Word, Excel, Outlook, and PowerPoint.

Nice to have

  • Pharmaceutical, biotech, clinical laboratory, GMP, or cGMP experience.
  • Experience with SOP creation and implementation, virology, and fibrology.

Culture & Benefits

  • Full-time laboratory role with either a Tuesday–Saturday first shift from 7:00 AM to 4:00 PM or a Monday–Friday second shift from 11:00 AM to 8:00 PM.
  • Work in a detail-oriented, team-based laboratory environment.
  • Follow ISO 17025, BSLT-2 cGMP, cGLP, A2LA, and quality control requirements.
  • Participate in educational programs covering laboratory functions, instruments, microorganisms, and troubleshooting.

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