Quality Assurance Specialist

🏢 Eva Pharma
📍 EgyptFull-timeOn-site
📅 Posted: 3w ago🔄 Updated: 3w ago
CV%
✨ AI Summary
EVA Pharma is seeking a Quality Assurance Specialist to join their team. The role involves monitoring environmental conditions, participating in raw material dispensing, overseeing manufacturing and packaging operations for GMP and SOP adherence, reviewing batch records, and managing deviations and CAPAs. The ideal candidate will have a Bachelor's degree in Pharmacy and 0-2 years of experience in a pharmaceutical QA environment, with knowledge of cGMP, GDP, CAPA, change control, quality documentation systems, ISO 9001, and validation principles.
Required Skills
Business, Sales & Management
Change ManagementQuality Systems
Engineering, Construction & Trades
ISO 9001ValidationCAPA
Other
GDP
Healthcare & Life Sciences
CGMP
Science & Research
Statistics
🎁 Benefits & Perks
Recognized and certified as a best place to work.
Requirements
Bachelor's degree in Pharmacy with 0-2 years of relevant experience in a pharmaceutical QA environment. Knowledge of cGMP and GDP principles, understanding of CAPA, change control, and quality documentation systems. Familiarity with ISO 9001 and safety programs, and awareness of validation principles and basic statistical concepts.
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 Specialist 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. Responsibilities: Monitor environmental conditions (temperature, humidity, pressure differentials) and ensure they comply with GMP requirements across production and warehouse areasParticipate in raw material dispensing and verify specifications and calculations as per SOPsOversee manufacturing and packaging operations to ensure adherence to GMP, SOPs, and data integrity requirementsReview batch records and logbooks for completeness, accuracy, and compliance with GDP (Good Documentation Practice)Record and report deviations, non-conformities, and incidents. Participate in root cause investigations and track corrective and preventive actions (CAPA)RequirementsBachelor's degree in Pharmacy0-2 years of relevant experience in a pharmaceutical QA environmentKnowledge of cGMP and GDP principlesUnderstanding of CAPA, change control, and quality documentation systemsFamiliarity with ISO 9001 and safety programsAwareness of validation principles and basic statistical concepts
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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