SEHA Salma Rehabilitation Hospital - ABU DHABI
Quality Officer & Senior Quality Officer
Location: Abu Dhabi
- Bachelor’s degree in healthcare administration, nursing or equivalent.
- CPHQ/ CPPS certified
- 3 years minimum experience as quality officer or senior quality officer from acute hospital or long-term care setting.
- Strong background in clinical risk management tools and activities.
- Led Quality Improvement projects and accreditation activities- JCI, CARF
-Experience in developing policies and procedures, clinical audit tools and audit related activities.
- Experience in developing KPIs and handling JAWDA KPIs.
I am very interested in this driver position at JM Foods. I have solid driving experience, good knowledge of road safety, and I am committed to professionalism and punctuality. I would appreciate the opportunity to be considered.
I am very interested in this driver position at JM Foods. I have solid driving experience, good knowledge of road safety, and I am committed to professionalism and punctuality. I would appreciate the opportunity to be considered.
I am very interested in this driver position at JM Foods. I have solid driving experience, good knowledge of road safety, and I am committed to professionalism and punctuality. I would appreciate the opportunity to be considered.
I am very interested in this driver position at JM Foods. I have solid driving experience, good knowledge of road safety, and I am committed to professionalism and punctuality. I would appreciate the opportunity to be considered.
I am very interested in this driver position at JM Foods. I have solid driving experience, good knowledge of road safety, and I am committed to professionalism and punctuality. I would appreciate the opportunity to be considered.
I am a pharmaceutical scientist who brings hands-on experience in aseptic manufacturing, regulatory compliance, and patient centered pharmacy practice. I have built my understanding across molecular docking, pharmacovigilance, and deviation management, always keeping medication safety at the core of my work. Supported validation projects and new product introductions while acquiring a Silver License in Aseptic processing for a Grade B area. Monitored equipment performance and promptly reported faults or issues to supervisors to minimize downtime. Performed manufacturing, filling, and packaging duties, ensuring full regulatory compliance with cGMP standards. Trained in internal audits, self-inspections, and CAPA processes through Thermo Fisher’s internal training modules. Operated bulking and aseptic filling lines in compliance with Standard Operating Procedures (SOPs), including line clearance and pre-fill checks in Grade A/B environments. Identified and reported non-conformance issues, contributing to investigations and corrective actions. Conducted SAP transactions and utilized Quality systems for GMP-related changes and report preparation. Performed aseptic interventions in isolators and RABS (Restricted Access Barrier Systems), maintaining first air integrity and unidirectional airflow. Additional training on QA/PQS- Deviation and CAPA management.
I am a pharmaceutical scientist who brings hands-on experience in aseptic manufacturing, regulatory compliance, and patient centered pharmacy practice. I have built my understanding across molecular docking, pharmacovigilance, and deviation management, always keeping medication safety at the core of my work. Supported validation projects and new product introductions while acquiring a Silver License in Aseptic processing for a Grade B area. Monitored equipment performance and promptly reported faults or issues to supervisors to minimize downtime. Performed manufacturing, filling, and packaging duties, ensuring full regulatory compliance with cGMP standards. Trained in internal audits, self-inspections, and CAPA processes through Thermo Fisher’s internal training modules. Operated bulking and aseptic filling lines in compliance with Standard Operating Procedures (SOPs), including line clearance and pre-fill checks in Grade A/B environments. Identified and reported non-conformance issues, contributing to investigations and corrective actions. Conducted SAP transactions and utilized Quality systems for GMP-related changes and report preparation. Performed aseptic interventions in isolators and RABS (Restricted Access Barrier Systems), maintaining first air integrity and unidirectional airflow. Additional training on QA/PQS- Deviation and CAPA management.
I am a pharmaceutical scientist who brings hands-on experience in aseptic manufacturing, regulatory compliance, and patient centered pharmacy practice. I have built my understanding across molecular docking, pharmacovigilance, and deviation management, always keeping medication safety at the core of my work. Supported validation projects and new product introductions while acquiring a Silver License in Aseptic processing for a Grade B area. Monitored equipment performance and promptly reported faults or issues to supervisors to minimize downtime. Performed manufacturing, filling, and packaging duties, ensuring full regulatory compliance with cGMP standards. Trained in internal audits, self-inspections, and CAPA processes through Thermo Fisher’s internal training modules. Operated bulking and aseptic filling lines in compliance with Standard Operating Procedures (SOPs), including line clearance and pre-fill checks in Grade A/B environments. Identified and reported non-conformance issues, contributing to investigations and corrective actions. Conducted SAP transactions and utilized Quality systems for GMP-related changes and report preparation. Performed aseptic interventions in isolators and RABS (Restricted Access Barrier Systems), maintaining first air integrity and unidirectional airflow. Additional training on QA/PQS- Deviation and CAPA management.
I am a pharmaceutical scientist who brings hands-on experience in aseptic manufacturing, regulatory compliance, and patient centered pharmacy practice. I have built my understanding across molecular docking, pharmacovigilance, and deviation management, always keeping medication safety at the core of my work. Supported validation projects and new product introductions while acquiring a Silver License in Aseptic processing for a Grade B area. Monitored equipment performance and promptly reported faults or issues to supervisors to minimize downtime. Performed manufacturing, filling, and packaging duties, ensuring full regulatory compliance with cGMP standards. Trained in internal audits, self-inspections, and CAPA processes through Thermo Fisher’s internal training modules. Operated bulking and aseptic filling lines in compliance with Standard Operating Procedures (SOPs), including line clearance and pre-fill checks in Grade A/B environments. Identified and reported non-conformance issues, contributing to investigations and corrective actions. Conducted SAP transactions and utilized Quality systems for GMP-related changes and report preparation. Performed aseptic interventions in isolators and RABS (Restricted Access Barrier Systems), maintaining first air integrity and unidirectional airflow. Additional training on QA/PQS- Deviation and CAPA management.
I am a pharmaceutical scientist who brings hands-on experience in aseptic manufacturing, regulatory compliance, and patient centered pharmacy practice. I have built my understanding across molecular docking, pharmacovigilance, and deviation management, always keeping medication safety at the core of my work. Supported validation projects and new product introductions while acquiring a Silver License in Aseptic processing for a Grade B area. Monitored equipment performance and promptly reported faults or issues to supervisors to minimize downtime. Performed manufacturing, filling, and packaging duties, ensuring full regulatory compliance with cGMP standards. Trained in internal audits, self-inspections, and CAPA processes through Thermo Fisher’s internal training modules. Operated bulking and aseptic filling lines in compliance with Standard Operating Procedures (SOPs), including line clearance and pre-fill checks in Grade A/B environments. Identified and reported non-conformance issues, contributing to investigations and corrective actions. Conducted SAP transactions and utilized Quality systems for GMP-related changes and report preparation. Performed aseptic interventions in isolators and RABS (Restricted Access Barrier Systems), maintaining first air integrity and unidirectional airflow. Additional training on QA/PQS- Deviation and CAPA management.