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Responsible for providing Regulatory CMC expertise into the development and implementation of the global regulatory strategy, operations and planning for the CMC aspects of assigned projects/products. Responsible for preparing and managing CMC regulatory
In this role, you will be a critical interface between regulatory strategy and commercial execution, ensuring that launch readiness, indication expansion initiatives, promotional and advertising materials for our medical device products comply
You are responsible for leading a range of global regulatory activities, encompassing both strategic and operational responsibilities across drug development, registration, and postmarketing phases. This role offers the opportunity to work in close
You will lead the development and execution of cutting-edge Chemistry, Manufacturing & Control (CMC) strategies, ensuring the highest standards of regulatory excellence across our diverse portfolio - from pharmaceuticals and medical devices to
In this role, you will coordinate and track regulatory submissions, partnering with the Regulatory Lead to prepare high-quality global submissions and ensuring timely delivery to health authorities worldwide. You will provide operational support to