# Quality Compliance Section Head

**Company:** [Eva Pharma](http://jobs.workable.com/companies/cVu9CoRuY1pLdxtN9NyNNA.md)
**Location:** Giza, Egypt
**Workplace:** on site
**Department:** Operations Business Division

[Apply for this job](http://jobs.workable.com/view/efb00be9-ad4c-48f3-bd2b-3490c36ecb15)

## 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.