صيدلي إنتاج

Company Description Ghonaim International CO (GIPCCO) is a growing pharmaceutical and cosmetic manufacturing company founded in 2016 by Mr. Al Saeed Al Ghoniam. The company is establishing a dedicated manufacturing facility in New Borg Al Arab City, Alexandria, Egypt, focused on sterile products such as IV solutions, vials, ampoules, and purified water. GIPCCO is strategically positioned in Block 15, Extension of the 4th Industrial Zone, to serve national and regional markets. Its strategy emphasizes IV solutions and sterile products aligned with the needs and market size of the Egyptian, Middle East, and African markets. The organization aims to build a modern, quality-driven manufacturing operation with strong growth potential for its team members.
Role Description The Production Pharmacist is responsible for overseeing and executing daily production activities for sterile pharmaceutical products and related cosmetic manufacturing lines. This full-time, on-site role in Alexandria, Egypt involves ensuring that production processes comply with Good Manufacturing Practices (GMP), quality standards, and regulatory requirements. Day-to-day tasks include supervising production steps for IV solutions, vials, ampoules, and purified water, monitoring equipment operation, and coordinating with quality control and quality assurance teams to maintain product integrity. The role also includes documenting production records, supporting validation and calibration activities, participating in deviation and incident investigations, and contributing to continuous improvement initiatives. The Production Pharmacist collaborates with cross-functional teams to optimize workflows, maintain safety standards, and support efficient, reliable output.
Qualifications

• Candidates should possess strong Pharmacy knowledge with a degree in Pharmacy or a related pharmaceutical science field, and understanding of sterile manufacturing and GMP.
• Candidates should possess skills in Production Management, including line supervision, workflow coordination, and familiarity with production planning and documentation.
• Candidates should possess skills in Quality Control, including in-process checks, sampling, and supporting laboratory testing aligned with established specifications.
• Candidates should possess skills in Quality Assurance, including adherence to SOPs, participation in audits, and support for validation, compliance, and continuous improvement.
• Candidates should possess effective Communication skills for working with cross-functional teams, reporting issues, training staff, and preparing clear documentation.
• Additional beneficial qualifications include experience in sterile or IV solution manufacturing, knowledge of safety and environmental regulations, strong problem-solving abilities, and proficiency in basic computer applications (e.g., MS Office).
• Ability to work in an on-site industrial environment, manage time effectively, and maintain high attention to detail under production timelines.