رهف وصفي

Participate in developing analytical procedures in stability testing to meet the required standards and specifications of each product under development.


Perform pharmaceutical analysis using a wide variety of techniques and equipments, complying with GLP, GMP, internal SOPs and Safety regulations.


Responsible for training and mentoring new laboratory fellows at the Analytical Method Development department

Experienced in stability testing of pharmaceutical and nutraceuticals products. Performed stability studies using specific analytical procedures to provide evidence of the quality of the R&D products over time.


Experienced in operating, implementing and calibrating laboratory analytical instruments such as HPLC, GC, Dissolution Apparatus, IR Spectroscopy, KF..etc


Was responsible for compiling data and stability findings to prepare a stability analysis report to be submitted to Regulatory Affairs .