Requirements
Bachelor's Degree in Health-related Sciences, with knowledge in Quality Management. Requires at least 2 years of experience in GMP environments and a Pharma background. Proficient in MS Office, with strong integrity, accuracy, reliability, organizational skills, attention to detail, and the ability to work independently and in groups. Must possess written and spoken English and Arabic.
Description
Job Title: Center Quality Assurance SpecialistDepartment /Sub-Department: Center Quality AssuranceDirect Manager: Center Quality ManagerWorkplace: Plasma CenterJob ObjectiveOne sentence summary of the main objective of the job, the most important activities and the means and guidelines to obtain the objectives.To perform Quality Assurance functions to ensure compliance with internal and external regulationsand protocol under the direct supervision of the Center Quality Manager (CQM).To edit SOP's relatedto processes at donor center level following the guidelines established according to Egyptianregulations and the guidelines established according to cMP requirements.EnvironmentInternal and external interactions i.e.: with other departments/divisions, international scope,providers, customers)Internal: Grifols Egypt for Plasma Derivatives (GEPD)plasma general management, especiallythe Director of quality, quality department of other GEPD plasma donor centers (DC).External: Donors, Health Authorities, government agencies.Key responsibilityTo 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 SOP's are followed.To assist to CQM in the edition of SOP's.To perform a review of the documentation of unsuitable test results and the disposition of theassociated units.Academic Experience RequiredBachelor's Degree in Health-related Sciences.Knowledge in Quality Management.Strong integrity and commitment to quality and compliance.Professional Experience RequiredPreferably at least 2 years of experience in a similar position, in environments of GoodManufacturing Practices (GMP) and Pharma background.Computing SkillsMs Office knowledge.Personal SkillsAbility to understand, explain, follow and enforce SOPs, protocols and other regulatoryguidelines.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.2 of 3Reference VersionStatus Effective dateTitleConfidential Information. It is not allowed the total or partial reproduction of this document without prior authorization.Printing Date PageGEPD-REC-000743 1.014-Jul-2025Center Quality Assurance Specialist Job DescriptionEffective03-Jun-2026 12:37 CESTCommunicates openly with CQM on issues noted during reviews and is able to give suggestionsfor 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.