Taha Abdulwanees

Production SupervisorFull Time

• Job Details:Ensure compliance with cGMP principles by performing in-process quality checks and participating in media fill activities during sterile injectable manufacturing. • Conduct deviations investigation to address non-conformities, propose corrective actions, and track CAPA implementations within the production line. • Collaborate in the preparation and review of Process/Facility/Equipment Risk Assessments, ensuring proper documentation and adherence to EU Annex-1 standards. • Perform routine in-process checks during sterile production/packaging, reviewing batch records and ensuring tests are properly captured for product quality control. • Revise and review in-process control documentation, conducting quality reviews of logbooks and ensuring SAP system data entry for batch testing and results. • Prepare Annual Product Quality Review reports and ensure compliance with audit requirements by participating in regulatory and internal audits.

Quality Assurance SpecialistFull Time

• Job Details:Managed and performed quality checks on incoming materials by confirming specifications and returning unacceptable materials for sterile production. • Performed line clearance and inspected materials before production/packaging activities, ensuring smooth operations and adherence to cGMP principles. • Assisted in the preparation of risk assessments, focusing on sterile product safety and regulatory compliance during production cycles. • Conducted internal audits and participated in regulatory inspections, providing detailed documentation and audit readiness for compliance with ISO and cGMP standards. • Developed and reviewed SOPs related to sterile manufacturing, ensuring compliance with in-process control and sterile injectable requirements