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Pharmacy Intern, Regulatory Sciences

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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Мэтч & Сопровод

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Описание вакансии

Текст:
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TL;DR
Pharmacy Intern, Regulatory Sciences (Regulatory Affairs): Supporting product applications, changes to product particulars, license renewals, and government tender submissions in Hong Kong with an accent on regulatory strategy, multidisciplinary collaboration, and medical functions. Focus on preparing regulatory materials, participating in cross-functional projects, and gaining practical experience through rotations in medical affairs, quality assurance, drug safety, and sales and marketing.

Location: Hong Kong – Quarry Bay

Company

hirify.global develops innovative therapies and works to translate scientific advances into compliant regulatory strategies that support medicine approvals and improved patient outcomes.

What you will do

  • Support new product applications, changes to product particulars, and license renewals across various disease areas.
  • Assist with government tender submissions and changes in particulars for the HA CPO.
  • Participate in assigned multidisciplinary regulatory science projects with guidance from a mentor and the team.
  • Rotate through Medical Affairs, Medical Information handling, Quality Assurance, Drug Safety, and Sales & Marketing.
  • Optionally gain exposure to Medical Compliance and Clinical Research.

Requirements

  • Bachelor’s degree in Pharmacy.
  • Strong attention to detail, organization, motivation, maturity, and teamwork.
  • Good interpersonal and communication skills.
  • Proficiency in Microsoft Office, especially Excel, Word, and PowerPoint.
  • Effective written and verbal communication skills in English and Chinese.

Nice to have

  • Prior knowledge of the local regulatory environment and regulations.

Culture & Benefits

  • Six-month internship with mentorship and structured functional rotations.
  • Collaborative environment that values diverse thinking.
  • Opportunity to gain industry experience across regulatory and medical functions.
  • Exposure to projects supporting the development and approval of innovative therapies.

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