Center Quality Assurance - Misr El Gedida
Posted
Summary
A Quality Assurance Specialist at Grifols' Egypt plasma-derivatives center maintains quality systems ensuring products and processes comply with SOPs and cGMP/regulatory requirements — reviewing GMP records, equipment QC and incident logs, releasing sample shipments and incoming supplies, and performing employee observations. Requires 2+ years in pharma QA/GMP environments.
The Quality Assurance (QA) Specialist is responsible for supporting and maintaining quality systems to ensure products and processes comply with internal procedures as well as local and international regulatory requirements.
Key responsibility
- Ensure SOPs and cGMP regulations are followed.
- To perform periodical review of DC GMP related records.
- To perform periodical equipment quality control review.
- To perform periodical review of equipment incident logs.
- To verify and release sample shipments.
- To inspect and release incoming supplies.
- To perform periodical employee observations.
Academic experience required
- Bachelor's Degree in Health-related Sciences. Preferably in Pharmacy.
- Knowledge in Quality Management.
- Strong integrity and commitment to quality and compliance.
Professional Experience Required
- At least 2 years of experience in Good Manufacturing Practices (GMP) environments in Quality Area within Pharma industry.
Computing Skills
- Ms Office knowledge.
- Personal Skills
- Ability to understand, explain, follow and enforce SOPs, protocols and other regulatory guidelines.
- Accuracy and reliability.
- Can work independently, excellent organizational skills, and attention to detail.
- Performs a high-level document review.
- Ability to work with cross functional areas.
- Good ability to identify problems and propose solutions.
Languages
- Intermediate level of written and spoken English
- Fluent in Arabic.