senior production specialist
Maro moheb
Production and Quality professional progressive experience across the Pharmaceutical, Cosmetics, and Medical Device industries, with a strong focus on manufacturing operations, process compliance, quality assurance, and continuous improvement. raw material inspection, and GMP standards. Holds a B.Sc. in Science and a Biochemistry Diploma, with hands-on expertise in audits, documentation, and ensuring product safety. Now seeking to apply and improve my skills in your role
About me
Production and Quality professional progressive experience across the Pharmaceutical, Cosmetics, and Medical Device industries, with a strong focus on manufacturing operations, process compliance, quality assurance, and continuous improvement. raw material inspection, and GMP standards. Holds a B.Sc. in Science and a Biochemistry Diploma, with hands-on expertise in audits, documentation, and ensuring product safety. Now seeking to apply and improve my skills in your role.
- Location
- October City, Egypt
- language
- English
Skills
- Soft Skills: Effective Communication
- Technical Leadership & Team Management
- Time Management & Work
- Scheduling
- Error Prevention & Attention to Detail
- Time Management & Multitasking
- Precision & Accuracy
- Team
- Collaboration
- Calm Under Pressure
- Strong Visual Inspection Ability
- Technical Skills: GMP & Lean Manufacturi
- Oracle APEX (Data Tracking & Reporting)
- Oracle ERP
- (Production & Inventory)
- Batch Manufacturing Records (BMR/BPR)
- Yield & Material Reconciliation
- OEE
- Optimization & Downtime Reduction
- Root Cause Analysis (RCA)
- Analytical Thinking & Problem-Solving
- Product
- Testing & Quality Assessment
- Staff Training & Development
- Continuous Improvement Strategies
- Decision-Making Under Pressure
- Proficient in MS Office (Excel
- Word
- PowerPoint)
- ADDITIONAL INFORMATION
- Military Status: Exempted
Experience
Jul 2026 — Present
Senior Production specialist
EVA cosmetics
October, Egypt Supervised and optimized high-speed filling and packaging lines for cosmetics and personal care products, ensuring maximum Overall Equipment Effectiveness (OEE). Performed precise yield calculations and material reconciliation audits for raw and packaging materials, keeping material variance at an absolute minimum and effectively eliminating documentation errors. Led troubleshooting initiatives and root cause analysis (RCA) for mechanical and operational line issues, significantly reducing downtime and maximizing output. Managed, mentored, and scheduled a team of technicians and operators, providing technical training to improve line safety, efficiency, and overall productivity. Maintained strict adherence to Good Manufacturing Practices (GMP), ISO quality standards, and health and safety (HSE) regulations across all assigned lines and batch processes. Utilized Oracle ERP and Oracle APEX to execute batch closures, track inventory movements, and generate accurate reconciliation reports
Mar 2025 — Jun 2026
Production specialist
Chemipharm for pharmaceutical industry
October, Egypt Oversee packaging operations in alignment with sops and production schedules, ensuring smooth machine performance and timely order completion. Inspect raw materials and packaging components to ensure quality standards, coordinating with QA for audits and compliance. Ensure safety protocols and PPE use, monitor cleanroom conditions, and report any safety or contamination risks. Improve efficiency by reducing waste, resolving technical issues, and training staff on packaging equipment and best practices. Maintain accurate production and materials records, and generate performance reports in compliance with regulatory requirements.
Mar 2023 — Feb 2025
Sterilization Chemist
Ultramed for Medical Device
Asyut, Egypt Oversaw end-to-end sterilization processes for medical devices, ensuring compliance with ISO and CE standards. Developed and implemented sterilization protocols and SOPs aligned with regulatory guidelines. Supervised equipment calibration and maintenance to ensure optimal sterilization performance. Trained and managed sterilization staff, ensuring strict adherence to safety and hygiene protocols. Conducted quality checks and audits, documented results, and led corrective actions for non-conformities. Performed final inspections of sterilized products, verifying packaging integrity and labeling for export compliance. Maintained detailed traceability records, including batch numbers, inspection data, and deviations. Prioritized export orders and implemented cost-saving measures, such as optimizing carton packaging capacity. Quality Control Analyst at Molding Section – Ultramed for Medical
Jan 2023 — Feb 2023
Quality Control Analyst at Molding Section
Ultramed for Medical Device
Monitored molding process parameters (temperature, pressure, cycle time) to ensure consistency and product quality. Conducted raw material checks before production to prevent defects. Performed visual inspections for surface flaws and used precision tools to verify part dimensions against specifications. Executed mechanical tests (tensile, compression, impact) to confirm physical properties. Identified and resolved issues with molding machines affecting output quality. Collected random samples for regular quality checks to detect process deviations early. Maintained accurate records of inspections, tests, and corrective actions for traceability. Performed root cause analysis on recurring defects and implemented preventive measures. Verified final molded parts met quality and design standards before release to next production stage. Quality Control Analyst at Catheters Section – Ultramed for Medical
Nov 2022 — Dec 2022
Quality Control Analyst at Catheters Section
Ultramed for Medical Device
Conducted inspections throughout catheter production, from tubing formation to final assembly. Performed visual and dimensional checks using precision tools to ensure defect-free, specification-compliant products. Carried out mechanical tests including tensile, burst, compression, flexibility, and durability assessments. Ensured compliance with ISO 13485. Maintained detailed QC records for audits and regulatory inspections. Suggested process improvements to enhance product quality and efficiency. Trained staff on QC procedures, inspection techniques, and safety protocols. Collaborated with R&D, production, and regulatory teams to resolve quality issues and align on standards. Enforced strict PPE use and hygiene practices to prevent contamination and ensure workplace safety.
Get in touch
- Phone
- +201224154804
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