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, 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 :
See Basic qualifications.
Why GSK? : We offer :
We offer :
When applying for this role, please use the 'cover letter' of the on-line application to describe how you meet the competencies for this role, as outlined in the job requirements above.
Thank you for your interest in this opportunity. The information that you have provided in your cover letter and CV will be used to assess your application.
Contact information :
You may apply for this position online by selecting the Apply now button.
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