Senior Regulatory Affaist Specialist

GlaxoSmithKline

Seoul, South Korea
Product registration
Life cycle management
Regulatory submissions
The job purpose is to manage product registration and the life cycle management of existing products, including timeline setup and regulatory planning for new products and indications

Job Summary

  • The job purpose is to manage product registration and the life cycle management of existing products, including timeline setup and regulatory planning for new products and indications.
  • Key responsibilities include planning regulatory affairs plans, establishing detailed registration plans, maintaining relationships with regulatory authorities and stakeholders, and managing regulatory updates for existing products.
  • GSK is a global biopharma company focused on uniting science, technology, and talent to get ahead of disease, aiming to positively impact the health of 2.5 billion people by the end of the decade.

Matching Summary

The job purpose is to manage product registration and the life cycle management of existing products, including timeline setup and regulatory planning for new products and indications.

Skills & Requirements

Must-have

  • product registration
  • life cycle management
  • regulatory submissions
  • regulatory agency guidelines
  • regulatory agency review process

Nice-to-have

  • agile working culture
  • inclusive workplace
  • ambitious for patients
  • accountable for impact

Key Requirements

  • Bachelor’s degree in pharmacy
  • Minimum 6+ years of experience in regulatory
  • Proficient English communication

Work Rights

Not specified

Tailored Resume

Cover Letter