Quality Compliance Section Head
Eva Pharma
| Company | Eva Pharma |
| Category | Operations & Admin |
| Location | Giza |
| Remote | On-site (inferred) |
| Employment | Not stated |
| Level | Lead |
| Salary | Not stated by the employer |
| Posted | 21 Jun 2026 |
| Last verified | 30 Jul 2026 |
| Source | Employer career page (workable) |
Description
Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members. Job Summary We are seeking a passionate and talented Quality Compliance Section Head to join our dynamic team. The ideal candidate will contribute to our mission of enhancing human health and well-being, ensuring that we meet the highest standards of excellence in our industry. Key Responsibilities: • Manage the site's deviation system, ensuring timely investigation, root cause analysis, and closure of quality events. • Oversee change control activities, ensuring all changes are properly assessed, approved, and implemented in compliance with GMP requirements. • Coordinate and review annual Product Quality Reviews (PQRs), analyze quality trends, and support continuous improvement initiatives. • Manage internal audits, support regulatory and customer inspections, and ensure timely closure of audit observations. • Review, monitor, and verify the effectiveness of CAPAs resulting from deviations, audits, complaints, and quality reviews. • Monitor quality compliance KPIs and prepare periodic reports for management. • Ensure GMP compliance across site operations and support inspection readiness activities. • Coach and support team members while promoting a strong quality culture across the site. Requirements • Bachelor's degree in Pharmacy. • 6–8 years of experience in Pharmaceutical Quality Assurance. • Previous experience in Quality Compliance, including deviations, change controls, audits, CAPAs, and PQRs. • Strong knowledge of GMP requirements and pharmaceutical quality systems. • Experience in handling regulatory inspections and audit activities is preferred. • Strong analytical, communication, and problem-solving skills.
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