Perform physical and chemical analysis of stability samples.
introducing of stability samples to storage facility to conduct stability
testing within one month of production.
stability samples on daily basis or when required to conduct physical and
of stability samples, including any outsourcing analysis, to ensure that
physical, chemical and microbiological quality attributes are within the acceptance
stability samples after analysis on weekly basis to comply with EHS
Report any OOS
to senior analyst to perform TROOS investigation.
validity of all reagents and working standards to comply with GLP.
shortage concerning reagents and working standards at the end of analysis to perform
shortage concerning consumable analysis tools (glassware, syringes, filters and
spare parts) at the end of analysis to perform purchase order.
weekly report about stability work done to complete KPI of stability
monitoring of stability chambers (temperature and humidity) to ensure
compliance with stability guidelines (WHO 2018 & MOH).
Bachelor of pharmaceutical science or Bachelor
years’ experience in the same field
Years of Experience:
20 March 2022
Application End Date:
14 April 2022
R&D - Stability