At Gulf Pharmaceutical Industries (Julphar), I prepare and issue Manufacturing Formula & Method, Manufacturing Directions, and Bills of Materials for commercial pharmaceutical products while maintaining cGMP and GDP compliance across production lines.
I manage SAP data change requests, including material codes, production versions, stage codes, BOM updates, and packaging records. I also lead Change Control, CAPA, deviation, risk assessment, and investigation activities in Ample Logic to close compliance gaps and strengthen audit readiness against ISO, FDA, and EMA standards.
Earlier, I supported packaging and labeling, insulin-plant administration, recruitment coordination, and ICDL training. I bring more than 11 years of regulated manufacturing, technical documentation, SAP administration, and cross-functional process improvement experience.
