# Quality Assurance Section Head

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

[Apply for this job](http://jobs.workable.com/view/6fe9207d-ea41-42a9-8e20-44f4762c341a)

## 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 Assurance 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:**

-   Lead the Quality Assurance activities related to **validation for both sterile and non-sterile operations**, ensuring all validation processes comply with regulatory and cGMP requirements.
-   Ensure the **planning, execution, and monitoring of validation activities** across manufacturing processes and systems.
-   Collaborate with manufacturing, engineering, and technical teams to ensure **validated processes are maintained and continuously improved**.
-   Conduct internal audits and assessments of validation activities, documentation, and systems to ensure compliance and identify areas for improvement.
-   Manage and coordinate **CAPA (Corrective and Preventive Action)** related to validation findings and quality issues, ensuring timely resolution.
-   Support **technology transfer and new product introduction**, ensuring validation requirements are properly implemented.
-   Lead training initiatives to enhance staff understanding of **validation practices, sterile and non-sterile operations, and cGMP requirements**.

## Requirements

-   Bachelor’s degree in Pharmacy, Chemistry, or a related field.

-   7–8 years of experience in Quality Assurance within the pharmaceutical industry, with strong expertise in validation activities for both sterile and non-sterile operations, including process validation, cleaning validation, and equipment qualification. Good understanding of cGMP and quality systems is required.
-   Experience in managing teams and leading audits, strong experience in managing diverse customer requirements, technology transfer projects, and setting timely communication with customers.
-   Excellent English, analytical, problem-solving, and communication skills.
-   Proven ability to lead diverse teams across multiple geographical regions.
-   Solid background in new product project management, technology transfer, and product launches in compliance with EU standards.