Quality Assurance Specialist

🏢 Eva Pharma
📍 Giza, EgyptFull-timeOn-site
📅 Posted: 9mo ago🔄 Updated: 9mo ago
CV%
✨ AI Summary
Quality Assurance Specialist needed in a pharmaceutical setting to ensure GMP/GDP compliance across production and warehouse areas. Responsibilities include monitoring environmental conditions, overseeing manufacturing and packaging operations for adherence to SOPs and data integrity, reviewing batch records, and recording deviations and incidents. The role requires a Bachelor's degree in Pharmacy and 0-2 years of QA experience, with knowledge of CAPA, change control, and quality documentation systems, as well as familiarity with ISO 9001 and validation principles.
Required Skills
Engineering, Construction & Trades
Geotechnical EngineeringCAPAISO 9001Validation
Information Technology
DevOpsTechnical Documentation
Finance, Legal & Governance
HR Compliance
Healthcare & Life Sciences
CGMP
Business, Sales & Management
Change Management
Science & Research
Statistics
Requirements
Bachelor's degree in Pharmacy.0-2 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
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)
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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