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3 часа назад

QC Associate II (Biotechnology)

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 Associate II (Biotechnology): Implementing and improving quality control methods for Twist DNA products in a high-throughput production laboratory with an accent on NGS, qPCR, fragment analysis, and data-driven release decisions. Focus on troubleshooting atypical results, supporting investigations and root cause analysis, reviewing CAPAs and deviations, and maintaining ISO/GDP-compliant quality documentation.

Location: USA - Portland, OR

Company

hirify.global produces DNA products supported by high-throughput laboratory quality control operations.

What you will do

  • Perform independent QC release for standard product families and verify compliance with customer specifications.
  • Execute and troubleshoot QC assays, including NGS, qPCR, fragment analysis, NanoDrop, and Qubit.
  • Initiate and follow up on nonconformances and quality events related to OOS, OOT, and atypical results.
  • Support impact assessments, investigations, and root cause analysis using 5-Why, Fishbone, and DMAIC techniques.
  • Review CAPAs and process deviations, monitor QC data, and assist with product and process quality reports.
  • Author and review SOPs, test methods, work instructions, and labels while maintaining batch, calibration, and inventory records.

Requirements

  • BS or MS degree in Biochemistry, Chemistry, Molecular Biology, or a related field.
  • At least 2 years of industrial experience in Operations or Quality Control.
  • Ability to make data-driven decisions and troubleshoot complex problems in a high-throughput environment.
  • Knowledge of molecular biology techniques, including PCR, cloning, and sequencing.
  • Excellent verbal and written communication skills.

Nice to have

  • Knowledge of Quality Control and Quality Assurance principles, including GMP and ISO.
  • Experience with analytical techniques such as spectroscopy and gel electrophoresis.
  • Experience with automated robotic systems and LIMS.

Culture & Benefits

  • Work in a production laboratory focused on continuous improvement of QC methods.
  • Maintain quality records and processes under ISO and GDP requirements.
  • Collaborate closely with the Operations team and report to the QC Manager.

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