Mohammed Saif Bashir

Support regulatory and GDP compliance activities within a licensed pharmaceutical distribution environment, ensuring alignment with MHRA requirements and internal quality systems. Maintain and manage controlled documentation including SOPs, quality records, and regulatory files in accordance with GxP standards. Assist with preparation for internal and external audits, supporting inspection readiness and documentation accuracy Contribute to deviation management and CAPA processes, ensuring timely investigation and resolution of quality and compliance issues. Collaborate with Responsible Person (RP) and cross-functional teams to support regulatory compliance across product handling and distribution activities. Support continuous improvement initiatives aimed at strengthening quality systems and regulatory processes Ensure accurate record keeping and documentation control within a GDP compliant environment. Develop working knowledge of pharmaceutical regulatory frameworks including GxP, GDP, and ICH guidelines.

Assisted in the regulatory aspects of pharmaceutical dispensing, ensuring compliance with legal requirements. Consistently processed 800 – 1200 prescriptions weekly, ensuring full compliance with GPhC regulations and accurate data entry to support patient safety and product traceability. Maintained 100% accuracy in prescription labeling and dosage checks over a 6-month audit cycle, demonstrating strong attention to detail and commitment to compliance. Applied Standard Operating Procedures (SOPs) and supported internal audits, demonstrating understanding of quality systems and regulatory expectations like those in GxP environments. Delivered excellent customer care, supporting 100+ patients daily with prescription queries, OTC advice, and product recommendations — balancing technical accuracy with communication skills under pressure.

Applied regulatory and quality control principles in a clinical laboratory setting, ensuring full compliance with Good Laboratory Practices (GLP) — a foundational standard for regulatory dossier development (e.g. CMC submissions). Participated in internal audits and quality reviews, gaining insight into regulatory inspection readiness and data governance. Used LIMS and Q-Pulse systems for accurate data entry, document control, and traceability — reflecting best practices for maintaining compliance with regulatory expectations. Maintained high standards of data integrity and documentation, ensuring accurate recording of sample handling and test results, directly relevant to regulatory review of M3 documentation. Identified minor inefficiencies in lab workflows and contributed suggestions to enhance process robustness, reflecting a commitment to continuous improvement and quality mindset.

Dispensed and labelled 250+ prescriptions weekly with 100% accuracy, ensuring full compliance with GPhC and MHRA standards. Advised 50+ customers daily on OTC medicines, following regulatory guidelines to support safe use and effective treatment. Managed stock for 300+ medicines, maintaining correct storage and documentation in line with Good Distribution Practice (GDP).