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6 часов назад

Reliability Engineering Intern (Pharmaceutical)

Формат работы
onsite
Тип работы
fulltime
Грейд
trainee
Английский
b2
Страна
Singapore
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
Reliability Engineering Intern (Pharmaceutical): Supporting equipment requalification, GMP documentation, SOP updates, facility reviews, and pest control compliance at a pharmaceutical site in Singapore with an accent on validation records, audit readiness, and corrective actions. Focus on coordinating IQ/OQ/PQ activities, maintaining controlled documentation, investigating compliance gaps, and assessing facility and environmental controls.

Location: City of Singapore

Company

hirify.global develops medicines and advances pharmaceutical science and healthcare outcomes.

What you will do

  • Plan, coordinate, and execute periodic equipment requalification activities, including IQ, OQ, and PQ where applicable.
  • Review and update requalification protocols, reports, and equipment calibration and validation records.
  • Review and update SOPs, initiate document change requests, and support document approval, version control, and archival.
  • Support GMP compliance activities, audits, deviation investigations, and CAPA implementation.
  • Conduct annual facility reviews covering facility conditions, utilities, and environmental controls.
  • Review pest control reports, monitor trends, coordinate with vendors, and maintain audit-ready documentation.

Requirements

  • Degree or diploma, preferably in a related field.
  • Students from polytechnic or university programmes are welcome to apply.
  • Strong organizational and time management skills, with the ability to manage multiple tasks simultaneously.
  • Excellent written and verbal communication skills.
  • Ability to work at the pharmaceutical site in Singapore.

Culture & Benefits

  • Exposure to engineering, production, validation, quality, and compliance functions.
  • Training in GMP requirements, equipment qualification, documentation, and audit readiness.
  • Equal opportunity workplace supporting diversity and inclusion.

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