Senior QP Delegate, CMC Development QA This is a great opportunity to contribute to the development of new innovative treatments for brain diseases, supporting
Exciting Career Opportunity in Regulatory Affairs Combination Products Do you dream of a career with a global pharmaceutical company built on life:changing
Senior QP Delegate, CMC Development QA This is a great opportunity to contribute to the development of new innovative treatments for brain diseases, supporting
Would you like to be part of a dynamic department responsible for ensuring the smooth operation of marketed products while bringing new treatments to market in
Do you want to use your strong quality mind:set and great interpersonal skills to make a difference within QA? Are you eager to play an important role in
Design Control Engineer/Specialist : CMC Biologics Device area Are you experienced with Design Control in late:phase and looking to join our growing team of
Are you passionate about ensuring fast and successful regulatory submissions and approvals for life:saving medicines? Do you possess a natural interest and
Do you want to use your strong quality mind:set and great interpersonal skills to make a difference within QA? Are you eager to play an important role in
Design Control Engineer/Specialist : CMC Biologics Device area Are you experienced with Design Control in late:phase and looking to join our growing team of
Do you have solid experience in project or line management within process and product understand:ing and/or within life cycle management processes or
Are you able to cut through complexity and drive regulatory strategies for high impact projects and would you like to work together with experts across
Do you want to use your strong quality mind:set and great interpersonal skills to make a difference within QA? Are you eager to play an important role in
Are you excited to be part of a dynamic and ever:evolving environment, contributing to Novo Nordisks purpose : Drive change to defeat serious chronic diseases?
Do you have experience from either RA, CMC, QA, and/or QC : or any other relevant area? Do you possess a natural interest and flair for regulatory guidelines?
Are you a specialist with a strong background in GMP and quality management in the pharmaceutical industry? Do you have a deep understanding in guidelines and
Do you have experience in CMC, QA, QC, RA or a related area? And can you offer a unique skill set : ideal for working with different stakeholders and
Do you want to drive and impact a variety of early and late:stage drug product development projects? Are you ready your project management experience and
In this job, 371 million people worldwide depend on you to develop the world's best drugs. Are you eager to work with complex problem:solving related to
Are you looking for an exciting opportunity within project management, due diligence, and business integration? Are you motivated by leading the complex
Are you ready to take on a key role in driving portfolio thinking and project excellence? Are you motivated by change, development, implementation, people and