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