1. Elaborate and conduct stability program according to the ICH and regulatory requirements.2. Ensure stability samples management: reception from manufacturing area, labelling prior initiation, entry and exit from stability chambers, distribution to the QC laboratory, destruction and inventory.3. Ensure that stability activities documentation is updated (SOPs,reports, CMC document, trends).4. Ensure that Data should be punched in Novatek sofware within a time.5. Ensure the date… Show more 1. Elaborate and conduct stability program according to the ICH and regulatory requirements.2. Ensure stability samples management: reception from manufacturing area, labelling prior initiation, entry and exit from stability chambers, distribution to the QC laboratory, destruction and inventory.3. Ensure that stability activities documentation is updated (SOPs,reports, CMC document, trends).4. Ensure that Data should be punched in Novatek sofware within a time.5. Ensure the date in and date out of the stability samples.6. Provide documentation support to QC personnel for creation and revision of laboratory documentation within the electronic document control and archiving system. Show less