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Global regulatory affairs lead — cmc, gmp, submissions

Dublin
Morgan Mckinley
Posted: 22 January
Offer description

A leading pharmaceutical company in Dublin is looking for a Regulatory Affairs Manager to lead regulatory activities at their manufacturing site. This role combines hands-on regulatory work with team leadership and compliance oversight. The ideal candidate should have over 7 years of experience in Regulatory CMC, strong knowledge of EU regulatory procedures, and a solid understanding of GMP. Join a collaborative environment that supports regulatory strategies across the organization.
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