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2 дня назад

Intern Quality Assurance (ED)

Формат работы
onsite
Тип работы
fulltime
Грейд
trainee
Английский
b2
Страна
China
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
Intern Quality Assurance (ED) (GLP/Quality Systems): Supporting nonclinical study oversight in a full-time, onsite Shanghai internship with an accent on GLP compliance, auditing, data integrity, and quality management systems. Focus on reviewing documents, managing SOPs, supporting deviation and CAPA processes, and preparing for regulatory inspections.

Location: SIMZ Pudong, Shanghai, China; full-time onsite

Company

hirify.global provides laboratory services, diagnostics, data, and technology solutions for healthcare providers, researchers, pharmaceutical companies, and patients.

What you will do

  • Learn and apply GLP regulations, compliance requirements, and quality management system principles.
  • Support document reviews, study audits, data integrity checks, and report reviews.
  • Assist with SOP lifecycle management and quality documentation practices.
  • Support deviation investigations, CAPA processes, risk-based quality oversight, and regulatory inspection readiness.
  • Collaborate with the Preclinical GLP Quality Assurance Department while developing analytical, communication, and problem-solving skills.

Requirements

  • Current enrollment in a bachelor's degree program in Pharmacy, Pharmaceutical Sciences, Toxicology, Veterinary Science, or Chemistry.
  • At least 3 months of experience using computer and office software applications such as Microsoft Word, Excel, and Outlook.
  • Strong organization, multitasking, communication, problem-solving, and critical-thinking skills.
  • Ability to work collaboratively in a high-performance team environment.
  • Available for a 20-week, full-time onsite internship in Shanghai from January to May 2027.

Nice to have

  • Good written and reading English proficiency, CET-4/6, and strong spoken English skills.
  • Interest in quality assurance, regulatory compliance, clinical research, or bioanalytical sciences.
  • Coursework or laboratory experience in biotechnology, pharmaceutical sciences, analytical chemistry, or biologics.
  • Exposure to GCP, GLP, regulated laboratory environments, data management systems, or quality management processes.
  • Experience with scientific data analysis.

Culture & Benefits

  • Paid internship with hands-on project work complementing academic studies.
  • Enterprise-wide learning experiences and access to professional development resources.
  • Leadership exposure, senior leader speaker sessions, and mentoring connections.
  • In-person workshops, intern cohort activities, and opportunities to connect with peers.
  • Exposure to hirify.global's inclusive culture, employee resource groups, and community initiatives.

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