Eva Pharma

Produces affordable medicines for global access

Quality Compliance Senior Specialist

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 Pharmaceutical Sciences is required.
Two to four years of experience in a similar position, with a proven track record in passing regulatory inspections, is required.
Fluency in spoken and written English is required.
Excellent knowledge of Microsoft Office Professional, including Word, Excel, PowerPoint, and MS Outlook, is required.
Strong communication and interpersonal skills, a results-oriented approach, teamwork ability, and resilience are required.

Responsibilities

Handle deviations according to the current procedure, including initial assessment, root cause investigation, root cause identification, and proposing corrective and preventive actions.
Handle changes within the site according to the Change Management SOP and follow up on associated actions.
Implement the Product Quality Review procedure and follow up on QMS CAPA closure and effectiveness checks.

Quality Compliance Senior Specialist

Eva Pharma · Giza, Egypt · Full-time · Posted 2025-08-31

Workplace: on_site

Department: Quality Assurance

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 Senior Specialist / Supervisor 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

Handling of deviations according to the current procedure including initial assessment, root cause investigation, root cause identification, and proposal of corrective & preventive actions.
Handling of changes within the site according to Change Management SOP along with the associated follow up of actions.
Implement Product Quality Review procedure and follow up of QMS CAPA closure and effectiveness check.

Requirements

Bachelor’s degree in Pharmaceutical Sciences.
2-4 years of experience in a similar position with proven track record in passing regulatory inspections.
Excellent communication and interpersonal skills, Result-oriented personality with team working ability & resilience.
Fluency in spoken & written English is required, Excellent knowledge of Microsoft Office Professional (word, Excel, PowerPoint, MS Outlook).

Apply

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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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