... strategy for site registration. Able to write and review of CTD Module 3.2.P Drug Product for new Marketing ... site documentation through change controls' management. Manage product life cycle maintenance e.g ...

... expertise to new product introduction project teams and different departments. Participating in change ... requirements. Experience in the pharmaceutical or medical device manufacturing company for over 3 years ...

... as core team member providing review and analysis of applicable regulatory guidelines and project ... experience Minimum 3 years’ related experience, including a minimum of two years regulatory experience ...