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Posted 15/10/2024 by CK Group- Science, Clinical and Technical
Management of post-approval activities for specified OTC products. Supports the EMEA Regulatory Affairs team for post-approval activities for MRP/DCP products across EEA and coordinate worksharing (WS) procedures for CMC and non-CMC variation, when WS is appropriate. Development of … more
Posted a week ago by Copello
Application of and compliance with, engineering processes and practices, including engineering framework, life cycle management and regulatory requirements. Identification of opportunities for the improvement of processes, practices and tools. Collaboration with discipline peers within the … more
