Location: Al Qastal Industrial Area, Amman, Jordan
Industry: Pharmaceutical Manufacturing
Job Summary:
Lead and oversee the effective implementation of assigned Quality Assurance systems and GMP compliance activities within the designated area, ensuring adherence to internal quality standards and regulatory requirements through strong technical oversight, process discipline, and cross-functional coordination.
Key Responsibilities:
Quality Systems Oversight:
- Oversee the implementation and effectiveness of assigned Quality Assurance systems (e.g., Change Control, CAPA, Deviations, Documentation Control, Supplier Qualification)
- Ensure compliance with internal procedures and regulatory requirements
GMP Compliance Monitoring:
- Ensure consistent application of GMP requirements across the assigned operational scope
- Identify compliance gaps and coordinate corrective actions with relevant stakeholders
Audit & Inspection Readiness:
- Plan, support, and participate in internal and external audits within the assigned scope
- Ensure timely closure of audit observations and readiness for regulatory inspections
Quality Review & Documentation Control:
- Review and approve quality-related documentation within delegated authority
- Ensure accuracy, completeness, and compliance of records across departments
Deviation, CAPA & Change Control Management:
- Oversee investigations, root cause analysis, and closure of deviations, CAPAs, and change controls
- Ensure effectiveness and sustainability of implemented actions
Team Coordination & Technical Guidance:
- Provide direction, technical guidance, and support to the section team
- Ensure priorities are managed effectively and deliverables are met
Training & Continuous Improvement:
- Support delivery of QA-related training programs within the assigned area
- Contribute to the continuous improvement of QA systems and processes based on audit findings and best practices
Cross-Functional Collaboration:
- Coordinate with Quality Compliance, Production, QC, Warehouse, Supply Chain, Engineering, and other functions
- Ensure quality requirements are integrated into operational processes.
Job Specification:
- Bachelor’s degree in industrial engineering, or a related field.
- Minimum of 8–10 years of relevant experience in Quality Assurance within a GMP-regulated pharmaceutical manufacturing environment. Strong experience in QA systems, including CAPA, deviations, audits, documentation control, and supplier qualification, is required. * * *
- Excellent command of English.
