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4 дня назад

QC Microbiology Associate II

27 - 88$
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
QC Microbiology Associate II (Microbiology/Quality Control): Performing microbiological testing and laboratory support for finished products, stability samples, environmental monitoring, and other samples with an accent on cGMP compliance, data integrity, and accurate documentation. Focus on reviewing laboratory results, maintaining and qualifying equipment, supporting investigations and continuous improvement, and operating safely in an FDA-regulated manufacturing environment.

Location: Onsite in Irvine, California, United States. Monday–Friday, 7:00 a.m.–3:30 p.m.; relocation is not available.

Salary: $27.88–$30.75 per hour

Company

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

What you will do

  • Perform microbiological testing on finished products, stability samples, environmental monitoring samples, and other laboratory samples.
  • Receive, prepare, process, document, review, and compile laboratory samples and results.
  • Maintain data integrity and compliance with cGMP requirements, approved procedures, specifications, and quality standards.
  • Support equipment calibration, qualification, preventive maintenance, troubleshooting, and routine laboratory operations.
  • Assist with laboratory investigations, procedure and test method updates, and continuous improvement initiatives.
  • Maintain laboratory cleanliness, organization, safety, and regulatory compliance.

Requirements

  • High school diploma or GED required.
  • At least one year of laboratory, microbiology, quality control, or related scientific experience.
  • Strong attention to detail and excellent documentation and recordkeeping skills.
  • Ability to follow written procedures and work independently and collaboratively in a regulated environment.
  • Proficiency in data recording, report preparation, and review of laboratory documentation.
  • Ability to work onsite in Irvine and adjust to non-standard hours when business needs require.

Nice to have

  • Bachelor’s degree in Microbiology, Biology, Chemistry, or a related scientific discipline.
  • Experience in pharmaceutical, biotechnology, medical device, or other FDA-regulated environments.
  • Familiarity with cGMP regulations, laboratory quality systems, and microbiological testing methods.
  • Experience with laboratory investigations, equipment qualification, or continuous improvement.

Culture & Benefits

  • Healthcare benefits and a 401(k) plan.
  • Tuition reimbursement.
  • Use of personal protective equipment and adherence to laboratory safety procedures.
  • Work in a laboratory and manufacturing support environment with exposure to biological materials, reagents, and controlled conditions.

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