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3 дня назад

QC Microbiology Associate I (Pharmaceutical Manufacturing)

23 - 28$
Формат работы
onsite
Тип работы
fulltime
Грейд
junior
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
QC Microbiology Associate I (Pharmaceutical Manufacturing): Performing routine microbiological testing and laboratory support for pharmaceutical products and manufacturing processes with an accent on environmental monitoring, microbial testing, cGMP compliance, and accurate documentation. Focus on investigating OOS/OOT results and laboratory deviations, maintaining qualified equipment, and improving microbiology test methods and SOPs.

Location: Onsite in Irvine, California, United States. Schedule: Sunday–Tuesday or Wednesday, 5:30 p.m.–5:30 a.m., working 3 or 4 12-hour shifts.

Salary: $23.68–$28.37 per hour.

Company

hirify.global develops and manufactures healthcare products and services focused on infusion therapy, pain management, nutrition, pharmacy compounding, wound care, ostomy care, and dialysis.

What you will do

  • Perform microbiological testing for finished products, stability studies, utilities, raw materials, and environmental monitoring samples.
  • Receive, prepare, incubate, enumerate, identify, and document microbiological samples and test results.
  • Record, review, and maintain laboratory data in accordance with cGMP, laboratory procedures, and data integrity standards.
  • Maintain laboratory equipment, media, reagents, and supplies to support uninterrupted testing.
  • Assist with equipment qualification, calibration, preventive maintenance, troubleshooting, and performance monitoring.
  • Support OOS, OOT, and laboratory deviation investigations, as well as improvements to test methods and SOPs.

Requirements

  • High school diploma or GED required; an associate degree in microbiology, biology, biotechnology, or a related discipline is preferred.
  • 0–2 years of experience in microbiology, laboratory, pharmaceutical, medical device, biotechnology, or another regulated environment.
  • Basic knowledge of microbiological techniques, aseptic practices, and laboratory safety procedures.
  • Ability to follow written procedures and accurately document laboratory activities.
  • Strong attention to detail, organization, teamwork, and ability to manage multiple priorities.
  • Basic computer proficiency, including Microsoft Office applications.

Nice to have

  • Experience in a cGMP-regulated pharmaceutical, medical device, or biotechnology environment.
  • Hands-on experience with environmental monitoring, bioburden testing, microbial identification, or sterility testing.
  • Familiarity with laboratory systems, data management software, electronic documentation, USP microbiological testing, and contamination control.

Culture & Benefits

  • Collaboration with Quality, Manufacturing, Technical Services, supervisors, and laboratory peers.
  • Work within a team-oriented environment focused on product quality, patient safety, and regulatory compliance.
  • Healthcare benefits and a 401(k) plan.
  • Tuition reimbursement.
  • Continuous improvement supported through hirify.global’s Sharing Expertise initiative.

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