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13 дней назад

Sr. Field Study Test Associate I (Medical Device Testing)

32 - 40$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
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
Sr. Field Study Test Associate I (Medical Device Testing): Supporting systems-focused field studies through end-to-end testing, technical troubleshooting, and validation of connected devices, mobile applications, and software-enabled workflows with an accent on real-world study readiness, system performance, and regulatory compliance. Focus on investigating system issues, executing study protocols, documenting diagnostic findings, and coordinating integrated testing across hardware, software, mobile, and cloud interfaces.

Location: On-site five days a week at the High Bluff office in California, United States

Base pay: $32.00–$40.00 per hour, plus bonus and benefits

Company

hirify.global develops and manufactures diabetes technology, including insulin pumps and connected software systems.

What you will do

  • Execute software and systems testing across connected devices, mobile applications, and integrated workflows.
  • Perform pre-study validation, smoke testing, configuration checks, connectivity validation, and readiness assessments.
  • Coordinate study setup, execution, monitoring, issue investigation, data collection, and closeout.
  • Collect diagnostic information, system logs, observations, test results, and other study documentation.
  • Support study protocols evaluating functionality, usability, performance, and interoperability across hardware, software, mobile, and cloud interfaces.
  • Collaborate with Systems Test, Software Engineering, Product, Clinical, Quality, and Project Management teams to resolve issues and improve study processes.

Requirements

  • High school diploma or GED.
  • 3+ years of experience supporting clinical research, medical device testing, system testing, product validation, or related activities.
  • 3+ years of experience in medical device testing, including experimental design and study protocol development and implementation.
  • Ability to execute study activities independently and complete tasks with minimal supervision.
  • Strong problem-solving, communication, documentation, organizational, and time-management skills.
  • Ability to work on-site five days a week at the High Bluff office.

Nice to have

  • Associate's or bachelor's degree in life sciences, clinical research, engineering, computer science, or a related field.
  • Familiarity with Good Clinical Practice, human subject research requirements, and applicable regulatory guidelines.
  • Familiarity with Tandem device systems and software- or systems-focused study activities.

Culture & Benefits

  • Bonus and a competitive benefits package.
  • Workplace focused on employee well-being, growth, collaboration, and inclusion.
  • Compliance with privacy, HIPAA, legal, and regulatory requirements.
  • Pre-employment drug screening and background check are required.

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