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2 дня назад

Associate Scientist I (Biotech)

Формат работы
onsite
Тип работы
fulltime
Грейд
junior
Английский
c1
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR

Associate Scientist I (Biotech): Designing and executing scientific experiments for assay development on the Luminex technology platform with an accent on molecular biology and biochemistry. Focus on laboratory data generation, nucleic acid extractions, and compliance with FDA/ISO quality standards.

Location: Onsite in Austin, Texas, USA

Company

hirify.global is a global leader in immunodiagnostic and molecular diagnostic solutions, advancing science to improve patient outcomes worldwide.

What you will do

  • Conduct day-to-day laboratory experiments including biological sample handling and nucleic acid extractions in a Biosafety Level II environment.
  • Design, execute, and interpret scientific experiments to develop assays based on Luminex technology.
  • Document experimental data in laboratory notebooks and present results to departmental and cross-site teams.
  • Write protocols and reports for feasibility, verification, and validation of molecular tests under quality system requirements.
  • Collaborate with Clinical Affairs, Design Transfer, Manufacturing, and Quality Control teams to meet project deliverables.
  • Assist in intellectual property development and ensure conformity to Design Control regulations and standards.

Requirements

  • Bachelor's degree in biological/chemical or related scientific disciplines, or an Associate's degree with at least 2 years of laboratory experience in molecular biology.
  • Knowledge of routine laboratory methods such as PCR, specimen handling, processing, and experimental documentation.
  • Must be based in or be able to work onsite in Austin, Texas.
  • High proficiency in oral and written communication and interpersonal skills.
  • Ability to handle pressure and meet tight deadlines.
  • Proficiency in Microsoft Word, Excel, and PowerPoint.

Nice to have

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

Culture & Benefits

  • Comprehensive rewards package including health benefits, retirement, and financial wellbeing.
  • Annual incentive program eligibility based on individual and organizational performance.
  • People-centered culture emphasizing accountability, inclusion, and continuous professional development.
  • Time off programs and wellbeing support.
  • Entrepreneurial environment that encourages speed and global collaboration.

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