Hend Abdullah Email & Phone Number

Cairo, Egypt

Cairo, Egypt

Communicate with Egyptian drug authority (EDA) for improvement of our products & its release Responsible for uploading data required for EDA to complete drug release Dealing with methodology department for method update according to latest EDA guidelines

Cairo, Egypt

-Managing regulatory requirements and audit support needs by completing & submitting accurate paperwork- Served as information systems, information services & end-users to make recommendations for optimization of systems.*Inspected, verified & documented quantifiable characteristics of finished goods by comparing against customer specifications & company quality standard.-Managing regulatory requirements and audit support needs by completing & submitting accurate paperwork- Served as information systems, information services & end-users to make recommendations for optimization of systems.*Inspected, verified & documented quantifiable characteristics of finished goods by comparing against customer specifications & company quality standard.-Responsible for all factory products annual review.

Cairo,Egypt

Environmental (Microbiologist) pharmacist-Dealing with all Production departments including sterile area doing its microbial validation, beside microbial check of all production areas.- Released reporting & record keeping to meet environmental regulations.-Followed safety standards & established SOPs.

Cairo,Egypt

Quality control specialist-Worked as Finished product specialist , responsible for analysis of drug according to Pharmacopeias dealing with (HPLC ,Karle Fischer ,Viscometer ,Hardness ,FriabilityUltraviolet spectrophotometer ,Dissolution &Disintegration)-responsible for S.O.P. updating data with Combination of Methodology, R&D master file ,validation & quality assurance & responsible for revision of lab. Certificates according to last update of (MOH).-responsible for ISO 17025 - making all its document making its application in the finished lab. & was responsible for chemical analysis of the drug belong to ISO 17025.- Document all expermental results in logbook & certificates .