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2 дня назад

Intern Quality Assurance (BioA)

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 (BioA) (Bioanalytical Quality Assurance): Supporting quality activities for regulated large- and small-molecule bioanalytical studies in a clinical laboratory with an accent on GCP, GLP, data integrity, and document control. Focus on reviewing study documentation and analytical data, maintaining QA systems and audit records, and learning how quality oversight supports clinical development programs.

Location: Onsite at SIMZ Pudong, Shanghai, China

Company

hirify.global provides laboratory services, diagnostics, data, and technology supporting healthcare, clinical research, pharmaceutical development, and patient care.

What you will do

  • Support Quality Assurance activities for bioanalytical studies conducted under GCP and GLP regulations.
  • Assist with reviewing study protocols, analytical data packages, reports, laboratory records, and other documentation under supervision.
  • Support data integrity assessments, compliance monitoring, quality audits, and inspection-readiness activities.
  • Maintain QA systems, training records, audit documentation, quality metrics, document control, and archival records.
  • Work with QA professionals and laboratory scientists to understand regulatory expectations and quality oversight.
  • Present a summary of the internship project, key learnings, and contributions at the end of the program.

Requirements

  • Current enrollment in a relevant bachelor’s degree program, including biology, biotechnology, biochemistry, immunology, medical laboratory science, pharmacy, pharmaceutical sciences, chemistry, or life sciences.
  • At least three months of experience using computer and office software applications, such as Microsoft Word, Excel, and Outlook.
  • Strong attention to detail, organizational, analytical, problem-solving, and critical-thinking skills.
  • Ability to work independently and collaboratively in a fast-paced, highly regulated environment.
  • Good written and reading English skills; passing CET-4 or CET-6 is preferred.
  • Availability for a 20-week full-time onsite internship from January 2027 through June 2027.

Nice to have

  • Basic knowledge of biological, biochemical, or pharmaceutical laboratory principles.
  • 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.
  • Interest in Quality Assurance, regulatory compliance, clinical research, or bioanalytical sciences.
  • Experience with scientific data analysis and effective written and verbal communication.

Culture & Benefits

  • Paid, immersive internship with hands-on work connected to academic studies.
  • Instruction, coaching, dedicated mentoring, and professional development support.
  • Enterprise-wide learning experiences, leadership exposure, and senior leader speaker sessions.
  • In-person workshops and opportunities to connect with the intern cohort and employee resource groups.
  • Access to LinkedIn Learning resources and development sessions.

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