Center Quality Assurance specialist

🏢 grifols egypt for plasma derivatives (gepd)
📍 EgyptFull-timeOn-site
📅 Posted: Today🔄 Updated: Today
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✨ AI Summary
The Center Quality Assurance Specialist will perform Quality Assurance functions to ensure compliance with internal and external regulations and protocols under the supervision of the Center Quality Manager. Key responsibilities include reviewing donor center records, equipment quality control, incident logs, sample shipments, and incoming supplies. The role also involves periodical employee observations, assisting the CQM in ensuring cGMP regulations and SOPs are followed, and editing SOPs. Additionally, the specialist will review documentation for unsuitable test results and disposition of associated units.
Required Skills
Healthcare & Life Sciences
CGMP
Business, Sales & Management
HR Management
Requirements
Requires a Bachelor's Degree in Health-related Sciences with knowledge in Quality Management. Must have strong integrity and commitment to quality and compliance. Proficiency in MS Office is necessary. Candidates must be able to understand, explain, follow and enforce SOPs, protocols, and regulatory guidelines, work independently with excellent organizational skills and attention to detail, and collaborate effectively in groups and with other departments. A good understanding of cGMP and quality systems, along with the ability to identify problems and propose solutions, is essential.
Description
JOB OBJECTIVE- To perform Quality Assurance functions to ensure compliance with internal and external regulations and protocol under the direct supervision of the Center Quality Manager (CQM).- To edit SOPs related to processes at donor center level following the guidelines established according to Egyptian regulations and the guidelines established according to cGMP requirements.KEY RESPONSIBILITIES- To perform periodical review of DC records.- To perform periodical equipment quality control review.- To perform periodical review of equipment incident logs.- To verify and release of sample shipments.- To inspect and release of incoming supplies.- To perform periodical employee observations.- To assist to CQM to ensure cGMP regulations are followed.- To assist to CQM to ensure that SOPs are followed.- To assist to CQM in the edition of SOPs.- To perform a review of the documentation of unsuitable test results and the disposition of the associated units.ACADEMIC EXPERIENCE REQUIRED- Bachelors Degree in Health-related Sciences.- Knowledge in Quality Management.- Strong integrity and commitment to quality and compliance.COMPUTING SKILLSMS Office knowledgePERSONAL SKILLS- Ability to understand, explain, follow and enforce SOPs, protocols and other regulatory guidelines.- Ability and willingness to study specific activities, in a short time.- Accuracy and reliability.- Can work independently, excellent organizational skills, and attention to detail.- Performs a higher-level document review and employee observations- Ability to work in groups and with other departments.- Communicates openly with CQM on issues noted during reviews and is able to give suggestions for corrections. Has a good understanding of cGMP and quality systems.- Good ability to identify problems and propose solutions.- Adherence to the Grifols skills and values.LANGUAGESWritten and spoken English and Arabic.
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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