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1 день назад

Associate Scientist I (Medtech)

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

Associate Scientist I (Medtech): Developing immunodiagnostic and molecular diagnostic assays with an accent on experimental design and biological sample analysis. Focus on implementing PCR methods, ensuring compliance with FDA and ISO standards, and generating high-quality experimental data.

Location: Onsite in Austin, Texas

Company

hirify.global is a global leader in immunodiagnostic and molecular diagnostic solutions dedicated to improving patient outcomes worldwide.

What you will do

  • Perform daily hands-on laboratory work, including nucleic acid extractions and biological sample handling in a Biosafety Level II environment.
  • Design, execute, and interpret scientific experiments to develop assays based on Luminex technology.
  • Generate, record, and analyze experimental data while maintaining detailed laboratory notebooks.
  • Write protocols and reports for the feasibility, verification, and validation of molecular tests.
  • Collaborate with Clinical Affairs, Design Transfer, Manufacturing, and Quality Control teams to meet deliverables.
  • Assist in the development of intellectual property and troubleshoot technical difficulties.

Requirements

  • Bachelor's degree in biological/chemical sciences or a related scientific field.
  • Associate's degree with at least 2 years of laboratory experience in molecular biology or biotechnology.
  • Knowledge of routine laboratory methods such as PCR, specimen handling, and experimental documentation.
  • Must be able to work onsite in Austin, Texas.
  • Strong oral and written communication skills.
  • Familiarity with mathematics and statistical analysis.

Nice to have

  • Working knowledge of ISO 13485:2016 standards and FDA regulations.
  • Prior experience in the medical device industry.
  • Knowledge of Design Control requirements per FDA Quality System guidelines.

Culture & Benefits

  • Comprehensive health benefits, retirement, and financial wellbeing plans.
  • Paid time off programs and wellbeing support.
  • Eligibility for an annual incentive program based on performance.
  • Entrepreneurial environment that values accountability, inclusion, and continuous development.
  • Opportunity to contribute directly to solutions that improve global patient care.

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