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4 часа назад

Technical Writer (Software Compliance)

Формат работы
remote (только Philippines)
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
Philippines
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
Technical Writer (Software Compliance): Translating business specifications into software validation, data migration, SOP, and user-support documentation with an accent on cGxP systems, regulatory compliance, and controlled-document practices. Focus on maintaining ACE system documentation, managing version-controlled review cycles, and creating Confluence-based onboarding and customer-support content.

Location: Remote, based in the Philippines; initial training requires a schedule compatible with U.S. standard working hours.

Company

hirify.global provides cloud-based quality management and regulatory compliance software for pharmaceutical, medical device, and other highly regulated industries.

What you will do

  • Translate business specifications into user documentation and maintain software and user-support documentation.
  • Draft, revise, and review software validation documents, including validation plans, configuration specifications, requirement specifications, and summary reports.
  • Maintain knowledge of ACE system functionality and support data migration documentation.
  • Draft and revise SOPs for internal and client use while updating approved document templates.
  • Manage documentation artifacts through review cycles, including version control, comment resolution, formatting, and file hygiene.
  • Use Confluence to create onboarding materials, FAQs, knowledge-base articles, and customer-facing documentation.

Requirements

  • Bachelor’s degree in a related STEM field or equivalent.
  • At least 2 years of technical writing experience related to software specifications and products.
  • Technical writing experience for cGxP systems or facilities, preferably in pharmaceuticals.
  • Knowledge of FDA regulations and experience with clinical and regulatory affairs documentation in a regulated environment.
  • Excellent verbal and written communication skills.
  • Strong organizational and analytical skills.

Culture & Benefits

  • Remote, full-time position based in the Philippines.
  • Initial training schedule compatible with U.S. standard working hours.
  • Employment with a multicultural team operating globally.
  • Coaching, professional development, and tools to support career growth.
  • Compensation and benefits structure designed to support employees.
  • Equal employment opportunity and non-discrimination commitment.

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