Eva Pharma

Produces affordable medicines for global access

Quality Assurance Section Head

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours

Full-timeGiza, El Omraniya, Giza Governorate, EgyptNo salary listedIn-person

About the Job

Requirements

A bachelor's degree in Pharmacy, Chemistry, or a related field.
Seven to eight years of Quality Assurance experience in the pharmaceutical industry, including validation for sterile and non-sterile operations, process validation, cleaning validation, and equipment qualification.
Strong expertise in validation activities and a good understanding of current Good Manufacturing Practices and quality systems.
Experience managing teams and leading audits.
Experience managing diverse customer requirements, technology transfer projects, and timely customer communication.
Excellent English skills.
Analytical, problem-solving, and communication skills.
Proven ability to lead diverse teams across multiple geographical regions.
A solid background in new product project management, technology transfer, and product launches in compliance with European Union standards.

Responsibilities

Lead Quality Assurance validation activities for sterile and non-sterile operations, ensuring compliance with regulatory requirements and current Good Manufacturing Practices.
Plan, execute, and monitor validation activities across manufacturing processes and systems.
Collaborate with manufacturing, engineering, and technical teams to maintain and continuously improve validated processes.
Conduct internal audits and assessments of validation activities, documentation, and systems to ensure compliance and identify areas for improvement.
Manage and coordinate corrective and preventive actions 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 on validation practices, sterile and non-sterile operations, and current Good Manufacturing Practices.

Quality Assurance Section Head

Eva Pharma · Giza, Egypt · Full-time · Posted 2025-10-28

Workplace: on_site

Department: Operations Business Division

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.

Apply

Apply at Eva Pharma

About the Company

Eva Pharma

Produces affordable medicines for global access

EVA Pharma develops and manufactures affordable medicines for global markets, focusing on 12 therapeutic areas such as anti-infectives, metabolic health, oncology, and pediatrics. It operates four manufacturing facilities with a 5,000-strong team and produces over one million healthcare products daily. The company runs two regional research centers that use AI-driven prediction and mRNA R&D to develop biological products and first-of-its-kind capabilities in the Middle East and Africa. EVA Pharma distributes its products to more than 60 countries and seeks to expand access to high-quality medicines worldwide. Its differentiation comes from its scale, regional R&D capabilities, and commitment to sustainable access, aiming to meet pressing, unmet disease needs with reliable supply.

Company size: 1,001-5,000
Company stage: Not listed
Total funding: Not listed
Headquarters: Al Sharikat, Egypt
Founded: 1997

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