Hiring.Camp

Center Quality Assurance Specialist - Tanta

Grifols Egypt For Plasma Derivatives

·

Jun 17, 2026

Location
Tanta
Type
Full-time
Department
IT
Experience
2+ years
Education
Bachelor
Closing date
Jul 18, 2026
Source
CareersPage

Description

Job Title: Center Quality Assurance Specialist

Department /Sub-Department: Center Quality Assurance

Direct Manager: Center Quality Manager

Workplace: Plasma Center

Job Objective

One 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 related

to processes at donor center level following the guidelines established according to Egyptian

regulations and the guidelines established according to cMP requirements.

Environment

Internal and external interactions i.e.: with other departments/divisions, international scope,

providers, customers)

Internal: Grifols Egypt for Plasma Derivatives (GEPD)plasma general management, especially

the Director of quality, quality department of other GEPD plasma donor centers (DC).

External: Donors, Health Authorities, government agencies.

Key responsibility

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 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 the

associated units.

Academic experience required

Bachelor's Degree in Health-related Sciences.

Knowledge in Quality Management.

Strong integrity and commitment to quality and compliance.

Professional Experience Required

Preferably at least 2 years of experience in a similar position, in environments of Good

Manufacturing Practices (GMP) and Pharma background.

Computing Skills

Ms Office knowledge.

Personal 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.

2 of 3

Reference Version

Status Effective date

Title

Confidential Information. It is not allowed the total or partial reproduction of this document without prior authorization.

Printing Date Page

GEPD-REC-000743 1.0

14-Jul-2025

Center Quality Assurance Specialist Job Description

Effective

03-Jun-2026 12:37 CEST

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.

Languages

Written and spoken English and Arabic.

Skills

GMPCompliance

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