Your Responsibilities :
The Global Regulatory Platform and Delivery team are creating new roles in the CMC Variations Poznan team. The purpose for the role will be leading or participating in global CMC Variation projects (for Pharma and Vaccines Products), timely maintenance of post approval CMC changes for Finished Product and Active Pharmaceutical Ingredients, providing expertise and support to Local Operating Companies with respect to post approval changes and responses to Regulatory Agency questions about Products.
Key responsibilities :
g. Europe (for Centralised, Mutual Recognition and Decentralised procedure submissions, US and International countries)
Basic qualifications :
Preferred qualifications :
Why GSK? : We offer :
We offer :
Thank you very much for your interest in development opportunities with GlaxoSmithKline.
Contact information :
You may apply for this position online by selecting the Apply now button.
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