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3 часа назад

QC Associate - Temp (Molecular Biology)

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 Associate - Temp (Molecular Biology): Performing routine QC release testing, product review, and analytical laboratory activities for molecular biology products with an accent on validated methods, data integrity, and ISO 13485:2016 compliance. Focus on executing qPCR, NGS, electrophoresis, and spectroscopic testing, investigating OOS/OOT results, and maintaining reliable QC records and instruments.

Location: Onsite in Wilsonville, Oregon, USA; Monday-Friday, 8:00 am-5:30 pm PT. Shift, weekend, holiday, or on-call coverage may be required.

Company

hirify.global develops biotechnology products supported by molecular biology and quality control laboratory operations.

What you will do

  • Perform routine QC release testing, data review, and basic product release activities under direct supervision.
  • Execute validated analytical methods, including qPCR, NanoDrop/Qubit measurements, fragment analysis, and basic NGS QC tasks.
  • Inspect incoming raw materials and prepare disposition recommendations for senior QC approval.
  • Support OOS and OOT investigations by gathering raw data, documenting findings, and escalating atypical results.
  • Maintain QC records, instrument logs, reagents, standards, assay controls, and laboratory inventory.
  • Perform environmental monitoring, water sampling, instrument maintenance, and continuous improvement activities as applicable.

Requirements

  • BS in Biochemistry, Chemistry, Molecular Biology, or a related field.
  • 0-2 years of industrial Operations/QC experience; internship, co-op, or relevant academic laboratory experience may substitute.
  • Knowledge of molecular biology techniques, including PCR, cloning, and sequencing, plus analytical methods such as spectroscopy and gel electrophoresis.
  • Basic laboratory skills, including pipetting, sample handling, and instrument operation; familiarity with LIMS.
  • Working knowledge of Good Manufacturing Practices and Good Documentation Practices.
  • Ability to work onsite in a laboratory, cleanroom, and manufacturing environment, including gowning and personal protective equipment requirements.

Nice to have

  • Hands-on experience with automated liquid-handling or robotic systems.
  • Experience with QC or QA operations in a regulated biotechnology or manufacturing environment.

Culture & Benefits

  • Fast-paced, team-oriented, and collaborative QC environment.
  • Work includes frequent standing, walking, repetitive pipetting, and lifting up to 25 lbs with or without reasonable accommodation.
  • Operations follow ISO 13485:2016, internal SOPs, ALCOA+ data integrity principles, and 21 CFR Part 11 requirements.

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