Omar Badran

Dulex Lab

• Site ManagerFull Time

  Jul 2021 - Present -3 yrs, 11 months

  • Job Details:Oversee daily operations Coordinate employee schedules, ensuring adequate coverage Enforce all workplace policies and procedures Coordinate training and professional development activities for employees Conduct staff performance reviews Maintain and adhere to departmental budget Approve project plans Address and report safety concerns in a timely manner Track and monitors project progress, adhering to prearranged standards Ensure compliance across the worksite Review all project contracts before submitting to management Answer inquiries from potential project partners Mediate on-site conflicts Prepare and submits bi-monthly progress reports
• QA /QC ManagerFull Time

  Nov 2019 - Jul 2021 -1 yr, 8 months

  • Job Details: Maintain robust food safety program (E.g. HACCP and pre-requisite programs)  Creation of QMS (Deviation, Compliant, documentation, Training, Change control, Material specifications, OOS, OOT, ...)  Design Error proof process to eliminate wastes and provide agile Supply chain  Close working and cooperation with other stakeholder to Embed quality culture  Pass National Food safety authorisation (NFSA) registration audit RFT  Lead, qualify and uplift capabilities of quality personnel (8 Members) through clear SMART plan to full fill gap in flexibility matrix  Create quality KPI’s and company scorecard  Lead Quality team in qualification of new Five production lines  Operation excellence and Lean Expert for Quality and production (Practical Problem Solving - PPS, Kaizen, 6S, 7 Waste and Tier process)

Astrazeneca

• Quality assurance Section headFull Time

  Jan 2018 - Nov 2019 -1 yr, 10 months

  • Job Details: Imported bulk review and release including data loggers review and evaluation ,Temperature Excursion assessment, Temperature Gap assessment, Excursion time and limit comparing with S- Life and submit any unsupported temperature excursion to global team, follow up closing each case and set CAPAs to avoid repeating  Deviation system owner - Deeply involved in all Production and QC lab investigation and deviation and approve all suppliers investigation  Change control system owner  Complaint system owner - Managing customer and Supplier complaints  QA supplier manager (Suppliers / contract manufacturers/ Contract Lab. and logistic service providers) - Contributes in Selection, Qualification - Create and approve of Quality assurance agreement (QAA) - Create and implement annual audit plan - Create audit report and work with suppliers to ensure implementation of CAPAs on time and ensure CAPA effectiveness  Internal audit system owner - Conducting internal audit to ensure appropriate implementation and compliance with global AstraZeneca standards, ISO 9001 standards, GMP, GDP, GSP and GLP Standards and local regulation standards  Ensure implementation and closing of External and Internal audit CAPAs on time and approve related effectiveness check of CAPAs  Qualified Person for release all AstraZeneca Products  Create annual quality training plan for Egypt site  Create budget plan (CAPEX and OPEX) for next Five years and follow up of monthly progress and utilization  Daily review and follow up on all Quality KPIs through Tier meeting  Monitor and report of all Quality KPIs on Monthly basis  Member of New product introduction team
• Quality Assurance SupervisorFull Time

  Jan 2016 - Dec 2017 -1 yr, 11 months

  • Job Details: Qualified Person for release all AstraZeneca Products to Egypt Market  Document control system owner – Create and approve of SOPs, instruction and SOMs  Managing product and material non-conformance investigations (OOS & OOT) and follow up for CAPA implementation and effectiveness  Reviewing instrument qualification documents  Conduction of regular checks through GEMBA Walk to ensure adherence of practices with GMP rules and data integrity requirements in Production areas and QC Lab
• Senior QC AnalystFull Time

  Jan 2014 - Dec 2015 -1 yr, 11 months

  • Job Details:• Develop the necessary Packaging, Process & Raw materials specification. • Project member in AZ New product introduction - NPI • Ensures appropriate implementation of good laboratory practice and data integrity • Qualified Person for release of manufactured product • Qualified Person for release of packaging material (PVC, PVDC, Hard Foil, Soft foil) and Active ingredient (APIs) • Lead 9 QC members (Finished product analyst, Microbiologist, packaging material analyst and Lab Sampler to achieve department and company KPIs
• QC Analyst & Site MicrobiologistFull Time

  Jan 2013 - Dec 2013 -11 months

  • Job Details:• Operation of QC Lab instruments :( HPLC, UV, IR, PH meter, Disintegration tester Dissolution, …) • Chemical and Microbiological analysis of finished products • Perform All Microbiological activities (water analysis, Hygiene monitoring, non-routine samples, Cleaning validation, ….)
• Production PharmacistFull Time

  Aug 2011 - Dec 2012 -1 yr, 4 months

  • Job Details:• Lead 34 employee to achieve department and company KPIs • Conduct GMP training for production team • Managing production Investigation, root cause analysis and CAPA • Support idea generation and quick wins in production areas