Category

Description

1. Develop, manage and control the Quality Unit strategy, plans, standard operating procedure, KPIs and ensure quality Unit goals and objectives achievement and the Quality Control/ QA and Validation Departments’ objectives and goals are met.
2. Monitor and manage all QA & Validation and QC yearly and quarterly plans, and update & amend QC and QA and Validation plans, objectives, goals according to the arising changes.
3. Plan, direct, monitor, and follow up QA, QC and validation activities. Ensuring proper coordination and synchronizations between the Quality Unit, Regulatory Affairs Department and the R&D Department.
4. Participating in designing, monitoring and maintenance of effective pharmaceutical quality system elements through complaints, deviations etc…
5. Monitoring and auditing work practices to ensure processes are being followed and products are reviewed/tested and inspected upon work process and standard operating procedure.
6. Monitoring adherence with GMP requirements and GLP requirements.
7. Monitoring adherence with safety rules within the facility, ensuring all safety and work hazards guidelines are being met.
8. Updating and following up responsibilities of direct reporting managers, monitoring their departments’ execution plans and KPIs achievement.

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