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Posted a week ago 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 Ultra Maritime
Manage and mentoring with technical direction to a team of System Engineers, allocating and managing their work. Ensure that both project and statutory requirements are met and works to improve the effectiveness of the systems design function within the company. … more
