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11 mo agofound 5 d ago

Quality Assurance Section Head

Eva Pharma·Giza, El Omraniya, Egypt·via workable
mid7+ yrsFull timecgmp
What the posting is about

Lead Quality Assurance activities for sterile and non-sterile operations, ensuring regulatory and cGMP compliance. Collaborate with cross-functional teams to maintain and improve validated processes. Conduct internal audits and manage CAPA. Support technology transfer and new product introduction. Train staff on validation practices and cGMP requirements.

Read out of the posting
Levelmid
Experience asked7+ years
EmploymentFull time
LocationGiza, El Omraniya, Egypt
RemoteNot stated
Visa sponsorshipNot stated
SalaryNot published, and most postings do not
Posted2025-10-28
Found viaworkable, direct from their system

We saw it 11 months after it went up.

The posting, as the company wrote it
Employment: Full-time Education: Bachelor's Degree 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.

Copied from Eva Pharma’s own board, not rewritten. Original ↗

Also open at Eva Pharma

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