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2 дня назад

Document Control And Validation Specialist (Medtech)

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
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

Document Control and Validation Specialist (Medtech): Managing controlled marketing documentation and validation processes within an eQMS environment with an accent on compliance, data accuracy, and cross-functional collaboration. Focus on developing validation test plans, maintaining quality records, and building BI dashboards to support regulatory and operational needs.

Location: Must be based in Manila, Philippines

Company

hirify.global is a leading digital healthcare company that combines wearable biosensors and cloud-based data analytics to detect, predict, and prevent cardiac disease.

What you will do

  • Coordinate controlled documents within the global Marketing system and maintain eQMS processes.
  • Develop and maintain validation documentation including test plans, scripts, and reports.
  • Ensure change orders are executed in a compliant and timely manner across cross-functional teams.
  • Support internal and external audits by managing document requests and quality records.
  • Design, build, and maintain dashboards and recurring reports to support business needs.
  • Collaborate with the Training coordinator to ensure change orders trigger required training.

Requirements

  • Must be based in Manila, Philippines
  • Must be available to work night shift (tentatively 8:00 pm - 5:00 am)
  • Bachelor’s degree or equivalent experience.
  • Minimum 5 years of experience in Document Management Systems or a combination of 2 years in Document Control and 3 years in a quality discipline.
  • Proficiency in Microsoft Office Suite, specifically advanced Excel formulas and pivot tables.
  • Experience with BI tools such as Tableau or Power BI.
  • Understanding of regulations for document control and experience in cGMP/GDP/GCP environments.

Nice to have

  • Previous experience with Veeva systems.
  • Experience in FDA-regulated industries.

Culture & Benefits

  • Opportunity to work in a mission-driven environment focused on improving cardiac health.
  • Collaborative and inclusive workplace culture.
  • Commitment to professional growth and career development.
  • Support for reasonable accommodations for qualified individuals with disabilities.

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