Supports UK, Ireland, Malta, Sweden, Finland, Norway, and Denmark products across the product
Supports the team with regulatory strategies (local and regional) that are in line with the
Supports the team with regulatory activities for National and/or European procedures
Prepares and compiles regulatory submissions, response to questions, renewals, post
Supports ad hoc projects (e.g., compliance reviews, audit preparation etc.)
Signs off on packaging material, leaflets, and SmPCs (as appropriate)

🎯 Requirements

Bachelor's/Master's degree in Life Science/Pharma
Minimum of 5 ~ 8 years of relevant work experience working within a Regulatory Affairs Department

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