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Regulatory Affairs Intern

MSD · Île de Hong Kong

New
Internship Junior 🇬🇧 English
Adverse Event Report Audits Compliance Collaborative Development Data Quality Assurance Document Control Systems Electronic Common Technical Document (eCTD) Employee Training Programs Pharmacovigilance Policy Implementation Product Registrations Records Retention Management Regulatory Affairs Compliance Regulatory Affairs Management Regulatory Applications Regulatory Communications Regulatory Compliance Regulatory Compliance Audits Regulatory Strategy Development Stakeholder Engagement Strategic Management Strategic Planning

Job description

About the role

This internship is part of the Pharmacy Internship Training Programme, supervised by the Regulatory Affairs Team. It is designed for recent graduates of local accredited Bachelor of Pharmacy programmes (HKU or CUHK) who wish to gain hands‑on experience in regulatory affairs, medical affairs and pharmacovigilance.

Key responsibilities

  • Assist with new product registration and lifecycle management, including strategic planning for launches and post‑approval variations.
  • Provide support to cross‑functional teams such as Tender and In‑Market Quality.
  • Participate in medical affairs activities, including handling inquiries, patient programmes, HCP visits and symposiums.
  • Support pharmacovigilance tasks, including adverse event reporting and data verification.
  • Attend drug‑office and medical‑device seminars and collaborate with stakeholders such as DOH officers, CPO and legal advisors.

Required profile

  • Graduate of a local accredited Bachelor of Pharmacy programme (HKU or CUHK).
  • Strong interest in regulatory affairs and willingness to work under supervision.
  • Ability to engage with cross‑functional teams and external stakeholders.

Required skills

  • Adverse Event Report
  • Audits Compliance
  • Collaborative Development
  • Data Quality Assurance
  • Document Control Systems
  • Electronic Common Technical Document (eCTD)
  • Employee Training Programs
  • Pharmacovigilance
  • Policy Implementation
  • Product Registrations
  • Records Retention Management
  • Regulatory Affairs Compliance
  • Regulatory Affairs Management
  • Regulatory Applications
  • Regulatory Communications
  • Regulatory Compliance
  • Regulatory Compliance Audits
  • Regulatory Strategy Development
  • Stakeholder Engagement
  • Strategic Management
  • Strategic Planning

What we offer

  • Structured training across regulatory, medical affairs and pharmacovigilance functions.
  • Opportunities to work with diverse internal and external stakeholders.
  • Exposure to real‑world product registration and lifecycle management processes.

Questions fréquentes

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Le contrat proposé est un Internship basé à Île de Hong Kong.

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Published 12 hours ago

Expires 1 month from now

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MSD

Île de Hong Kong