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50 минут назад

Microbiologist II - Non-Sterile (Biotech)

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 routine and complex microbiological testing for pharmaceutical and biochemical samples with an accent on product safety, regulatory compliance, and accurate documentation. Focus on method suitability, microbial identification, validation support, trend reporting, equipment troubleshooting, and mentoring microbiology staff.

Location: Tampa, Florida, United States

Company

hirify.global provides preparation and quality control testing for sterility, bacterial endotoxins, microbial detection, beyond-use dating, and active ingredient potency.

What you will do

  • Perform routine and complex microbiological testing, interpret results, and determine pass/fail status.
  • Prepare samples, reagents, media, and microbial stocks, including aseptic production and quality control of BSL-1 and BSL-2 materials.
  • Investigate unexpected results, identify microbiological trends, and support method suitability, method development, and validation activities.
  • Maintain laboratory documentation, chain-of-custody records, SOPs, equipment readiness, and biohazard waste disposal in compliance with applicable standards.
  • Support laboratory and safety audits, troubleshoot assigned equipment, and provide technical backup across workstations.
  • Lead special projects and train or mentor microbiology staff as needed.

Requirements

  • Bachelor’s degree in microbiology or a related science field with at least 12 semester hours of hands-on microbiology and/or chemistry laboratory coursework, plus 3–5 years of pharmaceutical or biochemical QC laboratory experience; alternatively, a master’s degree with 2–3 years of relevant experience.
  • Experience with microbiological laboratory functions such as microbial enumeration, growth promotion testing, streaking for isolation, environmental monitoring, method suitability, microbial identification, Gram staining, pipetting, or SOP revisions.
  • Working knowledge of microbiology principles, USP, cGMP, ISO 17025, cGLP, A2LA requirements, and quality control guidelines.
  • Ability to work independently with minimal supervision, solve routine and non-routine laboratory problems, multitask, and maintain accurate testing and documentation.
  • Intermediate Microsoft Office skills, including Word, Excel, Outlook, and PowerPoint, along with strong analytical, decision-making, communication, and interpersonal skills.
  • Ability to follow laboratory safety rules and SOPs when handling regulated BSL-1 and BSL-2 microorganisms.

Nice to have

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

Culture & Benefits

  • Full-time position with occasional overtime and weekend hours.
  • Participation in technical training and cross-technology educational programs.
  • Collaborative, detail-oriented environment focused on customer service, laboratory quality, and continuous learning.
  • Opportunity to contribute to special projects and laboratory compliance and safety audits.

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