Regulatory Affairs Manager - CMC

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THE FORCE CT GmbH

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Outsourcing • Consulting • Healthcare • Pharmaceuticals • Quality Management

51 - 200

Description

• You are in the swim in all topics related to CTD Module 3, e.g. development projects, life cycle measures such as technology transfers. • Your experience allows you to handle regulatory submissions (including eCTD publishing) swimmingly. • Global and/or European projects aren’t unchartered waters to you. • You bring along an ocean of knowledge when it comes to CMC guidelines in the EU and beyond. • Also elegantly circumnavigate the pitfalls of biotechnologically produced pharmaceuticals. • Your business fluency in German enables you to provide our international customers with the best possible support in the German market.

Requirements

• An academic degree in pharmacy or related scientific field prevents you from being in deep waters. • Your strong communication skills as well as your oral and written proficiency in English and German won’t let you drown when it comes to working with co-workers and customers alike. • Your strong project management skills help everyone to get their head out of water. • As an excellent team worker, cooperation is nothing you have to flounder through. • Instead of having scales on your eyes, an eye for detail completes your skills.