Regulatory Affairs Manager (Parallel Import)
Kent, England, United Kingdom
Hybrid / WFH Options
Hybrid / WFH Options
Cpl Life Sciences
to stakeholders. Submit variations (1a, 1b and type 2) timely. Develop strategies for regulatory submissions in coordination with stakeholders Collaborate with cross-functional teams (QA) to ensure compliance with regulations Maintain current knowledge of regulations, guidelines, and standards Management of packaging components stock levels. Skills … A degree in a related field least 4+ years of experience working in the Regulatory Affairs sector Previous experience in Parallel Imports Understanding of quality assurance principles in parallel imports Strong written and verbal communication skills Able to work independently and in a team environment Please note to apply for more »
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