Quality Assurance IPC Professional

🏢 Eva Pharma
📍 EgyptFull-timeOn-site
📅 Posted: 4w ago🔄 Updated: 4w ago
CV%
✨ AI Summary
EVA Pharma is seeking a Quality Assurance IPC Professional to ensure GMP requirements for production areas, manage calibration reports, and oversee the implementation of regulations. The role involves reviewing QC sampling plans, manufacturing batch records, and executing CAPA for incidents and non-conformities. The ideal candidate will have a Bachelor's degree in Pharmaceutical Sciences or Science and 5-8 years of experience in cGMP, Cross Contamination prevention, documentation, and change control management.
Required Skills
Engineering, Construction & Trades
CAPA
Healthcare & Life Sciences
CGMP
Other
Prevention of Cross Contamination
🎁 Benefits & Perks
Recognized and certified as a best place to work, supportive and innovative environment.
Requirements
Requires a Bachelor's Degree in Pharmaceutical Sciences or Science with 5-8 years of experience in cGMP, Prevention of Cross Contamination, cGMP Documentation (SOP), and CAPA & Change Control Management System.
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 Assurance IPC Professional 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:Assure the acceptance of the environmental conditions (Temp. %RH, ΔP) compliance with GMP requirements for all production areas and according to its classification, and the calibration and verification reports of all measuring devices Assure GMP & system implementation of regulations and instructions related to the application of procedures on daily basis and providing related reports accordingly, with verifying the batch records and logbooks completeness and guarantee of all data recordedReview, modify (if needed) and follow up QC sampling Plan of intermediates and finished products for each batch to obtain representative samples requiredReview the executed manufacturing batch records for completeness, correctness, compliance of in-process control results with specification and Execute CAPA of unusual incidents or non-ConformityRequirementsBachelor Degree in Pharmaceutical Sciences or Science 5-8 years Of experience cGMP and Prevention of Cross Contamination. cGMP Documentation (Sop). CAPA & Change Control Management System. 
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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