KHALED AL-FAR

• To manage and direct all activities' of quality control and Research and developments department
• To ensure optimal quality control department resources management, performance and allocation
• To follow documentation activities within the quality control
• To ensure proper planning, control and performance of all quality control activities
• To ensure that quality control department objectives fulfill the production and development plans
• To manage all analysis activities related to starting materials and finished products
• To control activities of long-term stability programs
• To decide on the factory contamination
• Investigated issues affecting group operations, prepared reports and helped correct problems.
• Established clear budgets and cost controls strategies to meet objectives.

Developing analysis methods for preparations in various pharmaceutical forms, such as ,Oral pharmaceutical , Solid dosage forms(Tablets, Capsules, Syrups, Suspensions, Mouth Wash, Oral drops)

Intramuscular injection, intravenous injection ( IV Bolus, IV injection), Subcutaneous injection , intradermal injection .

Suppositories and local dosage forms ( Cream, Lotion , Local sprays Vaginal douche.

supervise the testing and release of pharmaceutical products, raw materials, and stability samples on a timely basis. Responsible for talent development and retention of junior staff.

Responsible for technical development and empowering of staff and holding them accountable for activities required to meet deadlines.

Manage overall testing and release functions of QC laboratory.

Provide evaluation of the overall validity of the analytical results reported.

generate certificate of analysis and review stability reports.

Review and approve investigations (OOS, OOT), CAPA, Non- conformity (deviations), Supplier qualification process and effectiveness checks.

· Accountable for cGMP compliance of laboratory.

· Participate on project teams, third party audits, and regulatory audits.

· Audits quality control of raw materials, packaging components, labels and finished products to ensure compliance with established specifications and regulatory standards.

· Follows up with implemented programs to ensure compliance by all employees and other personnel in the manufacturing facility.

• Planned research activities to develop new processes, products and applications.

• Created and issued Standard Operating Procedures for team
• Measured and monitored quality performance against agreed KPI's, implementing recommendations as needed.
• Defined corrective actions for non-conforming products and complaints for continued quality improvements.
• Investigated customer complaints to address areas of improvement, eliminate non-conformance and increase customer satisfaction.
• Successful analyzed sample of Raw material , Bulk, FP with quality standard by variety's of analytical techniques include spectroscopy chromatography and titration to analyze sample..