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825 Glaxo Wellcome Manufacturing Pte

Regulatory Affairs Specialist (Replacement of maternity leave, 2Y Contract)

Korea - Seoulonsitemid

Posted today · via Workday

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About this role

JOB PURPOSE Lifecycle Management of Existing Products Plan, prepare, and submit regulatory variations for marketed products, including CMC changes, labeling updates, and maintenance of product licenses, ensuring ongoing regulatory compliance. Support for Regional and Global Regulatory Projects Manage and execute assigned regulatory projects and activities requested by regional and global stakeholders, ensuring timely delivery and alignment with business objectives. Regulatory Issue Management Identify, assess, and address regulatory issues related to assigned products, providing regulatory guidance and coordinating with internal and external stakeholders as needed.…

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1

Skills match

We compare your skills against the role requirements.

2

Level fit

This role is mid-level. We check your trajectory against it.

3

Domain experience

Your work in the role's domain matters more than your years total. We weight recent and direct experience.

4

Recency

A skill you used last quarter weighs more than one from five years ago. We grade on recency, not lifetime.

5

Location fit

This role is based in Korea - Seoul. We weight your proximity and willingness to relocate.

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