Certified Lean Six Sigma Black Belt
Liquids Section Head, Pharco Pharmaceuticals, September 2017 – Present.
o Participation in the startup of Povidone Iodine Department till the approval from Legal authorities.
o Leading teams on process improvement projects by using the Six Sigma methodology and Developing and maintaining Lean manufacturing/ Six Sigma theories and principles into practical applications.
o Translating production requirements into daily work schedule and direct staff in various departments in the execution of the work to meet production requirements as per schedule.
o Providing a leadership style to the team that encourages pride in work, team participation and personal development.
o Performing monthly coaching's and annual performance evaluations providing sufficient detail and examples for each employee.
o Ensuring staff is trained and adhere to Health & Safety procedures, GMP and SOP regulations.
o Liaising with other internal departments (Maintenance, Corporate Engineering, Technical Services, Quality Assurance) to solve production related problems.
Production Pharmacist, Sanofi Egypt, May 2015 – August 2017.
o In New oral Liquid Plant, July 2016 – Present, Supervising production activities concerning manufacturing of syrup, suspensions and Elixirs in preparation, filling and packaging sections.
o Performed 6 months rotation in Solid dosage forms section, January 2016 – June 2016. Supervising production activities including granulation, Compression, Coating and Capsule units.
o In Liquids, Semisolids and Suppositories Sections, May 2015 – December 2015. Supervising production activities during Preparation and filling processes.
o Active participation in the startup of the new oral liquids plant till the approval from legal authorities.
Quality Assurance Officer, Multi-Apex Pharma, November 2014 - April 2015.
o Implementation and following up applying of cGMP guidelines in all quality related departments in the factory.
o Following up dispensing process and activities in the dispensing room and ensuring its compliance with cGMP guidelines.
o Following up manufacturing processes of solid dosage forms including Tablets and Capsules.
o Following up manufacturing processes of liquid and semi-solid dosage forms including Syrup, Suspension, Shampoo, Cream and Suppository.
o Following up packaging processes in packaging area.
o Participation in Handling and follow-up of GMP Compliance activities including: Deviations and CAPA’s, Changes through following change control procedures, Out of limit investigations and Complaints investigations.
o Manufacturing and Packaging Batch Review & Batch release.
o New Leaflets and Boxes data reviewing.
Production Pharmacist, Sigma pharmaceutical Industries, March 2011 – October 2014.
o Supervising Production activities in Liquid section including syrup, suspension and liquids for external use in preparation and filling units.
o Supervising Production activities in the New Semisolid section including ointments, gels & creams in preparation, filling & packaging units.
o Providing the necessary planning, organization, and coordination of manufacturing activities to effectively drive production operations.
o Training, developing and coaching my team to high performance levels.
o Providing job specific training to all manufacturing operators within my area, verifying training records are up to date/accurate, and ensure all training requirements are compliant with cGMP and Safety regulations.
o Providing technical advice and guidance to manufacturing operators to ensure the effective and timely troubleshooting of processes and equipment.
o Assisting in the investigation process.
o Ensuring Manufacturing operations within their scope are in compliance with GMP and regulatory requirements.
Production Specialist, Delta Pharma, May 2010 - February 2011.
o In Liquid section including syrup, suspension, drops and liquids for external use in preparation and filling units.
o In Semisolid section including ointments, creams & suppositories in preparation and filling units.
