Summary
Overview
Work History
Education
Skills
Websites
Certification
References
Timeline
Generic

HEND ABDULLAH MOHAMMED

Shoubra

Summary

To continue my successful career path in the fast growing, well established Industry interacting knowledge & experience Dramatically impacting company growth through adding value to The Organization & the working groups Skills and abilities

Overview

1
1
Certification

Work History

supervisor in QC

Memphis Pharmaceutical & Chemical Industries
02.2024
  • Responsible for developing and implementing QA strategies in QC department, especially (Raw material Lab.) to ensure compliance with all applicable requirements, understanding regulatory requirements and recommending specific activities and resources required to support these strategies
  • Managing regulatory requirements and audit support needs by completing & submitting accurate paperwork.

supervisor in QA

Memphis Pharmaceutical & Chemical Industries
01.2022
  • Communicate with Egyptian drug authority (EDA) for improvement of our products & its release
  • Responsible for uploading data required for EDA to complete drug release to the market.

supervisor in Documentation department

Memphis Pharmaceutical & Chemical Industries
10.2016
  • Managing regulatory requirements and audit support needs by completing & submitting accurate paperwork
  • Complete deviation forms needed from all company sectors & make right investigation using 5 why method & fishbone diagram to implement procedural remedies
  • Making internal audit on all other departments of the company to check up all documents to still updated & continue good follow up
  • Completing change control forms needed from company departments
  • Responsible for making APQR (annual product quality review) & its charts to calculate CPk & check of OOT drugs, documenting & data control by providing regular updating of (SOP, batch records & protocols)
  • Following up Corrective actions & make sure that preventive actions has done in right way of external & internal audit 'CAPA' and make a tracking log for it, checking of OOS, risk assessment, KPI's & customer complains
  • Make sure that the suppliers that dealing with are qualified by auditing & continuous monitoring of their work
  • Follow up & check all labs Excel validation sheet application
  • Performing all work concerning secondary packaging of (Aspirin protect) tablet of Bayer company, starting from revision of all shipment documents, check on working hours calculations, filing & archiving and sending all these data to Bayer for confirmation by emails.

Supervisor in QA department

Memphis Pharmaceutical & Chemical Industries
10.2015
  • Environmental (Microbiological) pharmacist, Dealing with all Production departments and sterile area doing its microbial validation using rodac, TSA & PIA, beside microbial check of all production areas
  • Released reporting & record keeping to meet environmental regulations
  • Followed safety standards & established SOPs
  • Performing annually check of environmental measurements of all the company to fulfill ISO
  • Making check of water in water station in the company by water microbial analysis
  • Making performance qualification of water & validation of sterile areas.

Analyst Specialist /finished product in QC department

Memphis Pharmaceutical & Chemical Industries
08.2008
  • Quality control specialist, Worked as Finished product specialist, responsible for analysis of drug according to Pharmacopeias dealing with (HPLC, KarliFischer, Viscometer, Hardness, Friability Ultraviolet 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 (EDA), doing all its document making its application in the finished lab
  • & was responsible for chemical analysis of the drug belong to ISO 17025.

Education

Bachelor degree - Pharmaceutical Sciences

Cairo university
Cairo, Egypt
05.2007

Skills

  • Organizational / managerial skills
  • Organizable co-operative Team oriented
  • Familiar with quality control methods and tools in the pharmaceutical industry
  • Decision making and problem solving
  • Follow updated regulations (WHO) & EDA requirements
  • Follow quality, health & safety rules to ensure safety of employees and products
  • Communication skills
  • Negotiation
  • Making public relations Experience exchange
  • Microsoft office skills
  • Photoshop & visual basic
  • Excellent data collection and analysis skills
  • QA Documentation and Compliance systems experience
  • Make sure that good investigation has done for deviations
  • Applying of change control documents immediately and follow up
  • Checkup & follow of APQR, complains, oot, oos & risk assessment
  • Make sure that CAPA has performed well & make follow up with tracking

Certification

  • EDA guidelines based on WHO
  • LSSGB( Lean six sigma green belt)
  • Documentation (Holdipharma)
  • HVAC (heat ventilation air conditioning)
  • Quality, Health, Safety, and Environment (QHSE)(Holdipharm)
  • Marketing diploma (Ads for media)
  • Strategy of content marketing (Coursera)
  • Marketing fundamental (Mharat mn Google)
  • Photoshop, visual basic, mud box, Maya & 3d max
  • Certificate of fundamental of digital marketing ( Maharat min google) (Marketing)

References

  • Quality assurance Section head Dr.Moushera
  • Quality control Section head Dr.Heba Samir
  • Raw material manager Dr.Nesreen Salah

Timeline

supervisor in QC

Memphis Pharmaceutical & Chemical Industries
02.2024

supervisor in QA

Memphis Pharmaceutical & Chemical Industries
01.2022

supervisor in Documentation department

Memphis Pharmaceutical & Chemical Industries
10.2016

Supervisor in QA department

Memphis Pharmaceutical & Chemical Industries
10.2015

Analyst Specialist /finished product in QC department

Memphis Pharmaceutical & Chemical Industries
08.2008

Bachelor degree - Pharmaceutical Sciences

Cairo university

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