This role involves managing all analytical aspects within responsible projects to ensure operational business compliance with cGMP, Quality Assurance Agreement, regulatory requirements and Novartis Quality Manual. The right candidate will be responsible for ensuring analytical Life Cycle Management for commercial products and timely analytical implementation for new projects.
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* Coordinates and manages analytical method transfers and stability studies.
* Compiles quality control monographs describing test procedures and specification setup.
* Oversees final dosage form testing for release and stability, as well as functional testing of medical devices.
* Provides scientific analytical support for quality control, production and registration.
* Presents and discusses analytical data in local and international project teams.
The ideal candidate should have approximately 5-8 years of experience in the pharmaceutical industry or analytical laboratory in a GMP environment. Knowledge of GMP, Quality Control (QC) Testing and Quality Standards is essential. Additionally, the candidate should possess strong project management and analytical expertise.
Novartis offers a competitive salary, attractive incentive program, modern company pension scheme, childcare facilities and learning and development opportunities. The company values diversity and inclusion, providing an outstanding working environment and diverse teams representative of patients and communities served.
We are open to part-time and job-sharing models, supporting flexible and remote working where possible. If you require adjustments during the recruitment process due to a medical condition, physical disability or neurodiverse condition, please contact us.