Quality Compliance Senior Specialist

🏢 Eva Pharma
📍 Giza, EgyptFull-timeOn-site
📅 Posted: 12mo ago🔄 Updated: 12mo ago
CV%
✨ AI Summary
The Quality Compliance Senior Specialist will contribute to maintaining high standards in pharmaceutical quality and compliance. Key responsibilities include handling deviations with root cause analysis and corrective/preventive actions, managing changes via Change Management SOP, and ensuring closure and effectiveness of CAPAs within the QMS. The role requires a Bachelor’s degree in Pharmaceutical Sciences and 2-4 years of experience with regulatory inspections, along with strong communication, teamwork, and proficiency in MS Office. Fluency in English is required.
Required Skills
Business, Sales & Management
Project ManagementHR ManagementChange Management
Engineering, Construction & Trades
Geotechnical EngineeringCAPA
Productivity & Workplace Tools
Microsoft Office
Soft Skills & Professional Competencies
CollaborationRoot Cause AnalysisCommunication
Finance, Legal & Governance
Audit Support
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).
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 SummaryWe 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.
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🎯 Overalli74%
⚡ Skillsi85%
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Ontology Match: 85.0
Matched:✓ Requirements Matching✓ Ontology Skills Mapping
📜 Eligibilityi49%
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Local: 19600%
🏗️ Career Fiti91%
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Seniority: 91.0
📋 Requirementsi67%
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Domain: 67.0
🔥 Motivationi78%
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Title Fit: 78.00