Quality Assurance Specialist at The National Co. for Manufacturing Aluminum Tubes – TUBE (2024-07 – Present)
- Ensuring the compliance of manufacturing processes with current Good Manufacturing Practices (cGMP).
- Responsible for managing, organizing, and controlling the flow of documents within an organization
- Updating SOP and reviewing its related documents and reports for document validation and approval, in addition to following up on internal and external audits to ensure compliance with quality standards and regulations, and conformity to quality standards (ISO 9001, ISO 14001).
- Conducted training sessions for operators on proper implementation of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) to ensure regulatory compliance.
- Actively involved in preparation, documentation, and follow-up for ISO (ISO 9001, ISO 14001) and GMP renewal audits, ensuring audit readiness and compliance.
- Prepared, reviewed, and maintained audit-related and compliance documentation in line with regulatory and customer expectations.
- BRCGS Certified for Packaging Materials, with practical experience in standard implementation and compliance.
IPC Specialist at Macro Group Pharmaceuticals (2021-10 – 2024-07)
- Perform in process control inspection in the production Area liquids and semi-solid lines.
- Review the batch records
- Create and update SOPs
- Report the Annual product review reports
- Control the Receiving and Dispensing of Raw and Packaging Materials.
- Follow up on Preparation, Filling & Packaging Processes.
- Participated in internal audits
- Review the work order for raw materials
- Ensure that all activities in his unit or section are done according to the relevant GMP and ISO standards (ISO 9001, ISO 14001, iso 45001).
- Participate in making a presentation periodically to explain new topics to colleagues and workers in the pharmaceutical industry.
