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1 день назад

QC Microbology Assoc II

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 Microbology Assoc II (Microbiology/Quality Control): Performing microbiological testing and laboratory support for pharmaceutical and medical products with an accent on cGMP compliance, sample handling, data integrity, and accurate documentation. Focus on testing finished products and environmental samples, maintaining laboratory equipment, verifying results, and supporting quality-system improvements in a regulated onsite environment.

Location: Onsite in Irvine, California, United States. Schedule: Sunday–Tuesday/Wednesday, 5:30 PM–5:30 AM, 3/4 x 12-hour shifts.

Company

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

What you will do

  • Perform microbiological testing of finished products, stability samples, environmental monitoring samples, and other laboratory samples.
  • Receive, prepare, process, document, review, and compile microbiological samples and results in accordance with cGMP requirements.
  • Support equipment calibration, qualification, preventive maintenance, troubleshooting, and routine laboratory operations.
  • Verify test results against approved procedures, methods, specifications, and quality standards.
  • Assist with improving laboratory procedures, test methods, documentation practices, cleanliness, and safety compliance.

Requirements

  • High school diploma or GED.
  • At least one year of laboratory, microbiology, quality control, or related scientific experience.
  • Strong attention to detail and proficiency in data recording, report preparation, and laboratory documentation review.
  • Ability to follow written procedures and work independently and collaboratively in a regulated environment.
  • Ability to work the specified overnight Sunday–Tuesday/Wednesday schedule and other non-standard hours as required.
  • Ability to stand, walk, bend, use laboratory equipment, and occasionally lift up to 20 pounds.

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, microbiological testing methods, investigations, equipment qualification, or continuous improvement.

Culture & Benefits

  • Healthcare benefits, a 401(k) plan, and tuition reimbursement.
  • Work in a laboratory and manufacturing-support environment with required PPE and safety procedures.
  • Participate in a culture focused on knowledge sharing, continuous improvement, healthcare quality, and patient safety.

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