Quality Assurance- IPC (Executive) Egypt

Egypt·Cairomid

OtherQuality Assurance

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Quick Summary

Requirements Summary

Bachelor’s degree in pharmacy. Experience: 3–7 years in sterile and non‑sterile manufacturing. Shift Flexibility: Ability to work night shifts is essential.

Technical Tools

OtherQuality Assurance

Jamjoom Pharma has rapidly emerged as one of the leading pharmaceutical companies in the Afrasia region. With a geographical focus on the Middle East, Africa, and CIS countries, our strategic emphasis on selected therapeutic categories has driven rapid growth, market acceptance, and overall success.

About the Role

~1 min read

We are seeking a dedicated Quality Assurance IPC (Executive) to ensure strict adherence to GMP standards and quality assurance systems across all facility areas. This role is critical to maintaining compliance, supporting production excellence, and embedding a strong quality mindset throughout operations.

Responsibilities

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IPC testing during all stages of product manufacturing in line with SOPs.
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Sampling of intermediate, bulk, and finished product batches for routine testing, validation, and cleaning.
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Monitoring and enforcing quality assurance measures in production areas, ensuring compliance with IPC testing.
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Implementing procedures for batch manufacturing and packaging documents, specifications, and SOPs.
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Overseeing QA measures during validation batches and planned changes.
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Monitoring calibration of production equipment and IPC instruments.
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Reviewing batch documentation for accuracy, completeness, and compliance.
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Reporting and following up on incidents, corrective actions, and CAPA implementation.
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Ensuring GMP standards are applied in warehouse, dispensing, manufacturing, and packaging areas.
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Participating in deviations, complaints, OOSs & OOTs, ensuring timely closure.
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Identifying and rejecting non‑conforming materials/products per GMP standards.
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Coaching operators to embed a quality mindset in daily activities.

Requirements

~1 min read

Education: Bachelor’s degree in pharmacy.
Experience: 3–7 years in sterile and non‑sterile manufacturing.
Shift Flexibility: Ability to work night shifts is essential.
Regulatory Knowledge: Up‑to‑date knowledge of GMP, EDA, SFDA requirements, WHO and ICH guidelines.
Systems Expertise: Preferable knowledge of SAP system.
Technical Skills: Experience with IQ, OQ, PQ protocols, facility/utilities management, equipment qualification, and strong background in cGMP/GLP compliance.
Language Proficiency: Excellent command of English, spoken and written.