QA Officer At Hikma Pharmaceuticals

Validation Supervisor At Hikma Pharmaceuticals Company

 Validation Supervisor At Hikma Pharmaceuticals Company 

Job Summary:Responsible for assisting a team of analysts, officers and/or technicians undertaking quality work. Job holders are involved in a full range of quality section responsibilities


Duties & Responsibilities:

  • Manages significant validation projects delivering agreed objectives and high level of resource utilization
  • Leads the validation area, monitor performance and ensure high standard of efficiency by managing employees’ workload and priorities to guarantee productivity and efficiency of out-puts
  • Participate in the decision making for issues concerning validation within the facility.
  • Communicate effectively with other departments to facilitate validation activities.
  • Reviewing validation master plan of the site.
  • Reviewing of products Process validation protocols & Cleaning validation and protocols.
  • Reviewing of Analytical method validation protocols and reports.
  • Reviewing of QC instruments qualification and calibration activities and plans.
  • Reviewing of Production machines, R&D machines qualification activities and protocols.
  • Reviewing of Facility utilities qualification activities and protocols.
  • Reviewing of Environmental Monitoring reports/trends..
  • Reviewing of media fill qualification activities and steps ((intervention, video revision, data sheet revision, report creation)
  • Reviewing of Computer system validation activities.
  • Conducts some aspects of validation training and carries out an ongoing review of the effectiveness of the training.


Job Qualifications:

  • 5- 8  year of successful experience (Sterile Area).
  • B.Sc. degree in Pharmacy, Science or Engineering.
  • Preferably (Cairo, Obour, New Cairo, Nasr City, Heliopolis, Badr, Zagazig, Sharqiyah, and 10th of Ramadan) residents

Location: Egypt


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