Quality Material Specialist

6 months ago


مصر, Egypt 00E1 - Grifols Egypt Plasma Der Full time

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

**Job Objective**
Quality Material Specialist is responsible to inspect, approve and release of incoming critical
supplies and associated documentation before being released to Donor Centers (DCs) and Plasma
Testing Laboratories. Quality Material Specialist identifies and document any deviation of
materials and ensure these deviations are corrected.

**Environment**
Internal: Laboratory Operations Manager, Laboratory Quality Assurance specialist, Laboratory
Quality Control specialist, Center Manager, Center Quality Manager, Logistics Manager, Logistics
Warehouse Keeper.
External: Auditors.

**Key responsibility**
To ensure the execution of Quality inspection, approval and release of incoming Materials and
associated documentation is done according to the established procedures.
To register the Quality process as per established procedures in the electronic material
management system.
To be in contact with Logistics Department for the receipt of softgoods in the warehouse.
To coordinate with QC Plasma Testing Laboratories and Donor Centers the release of incoming
supplies.
To register and inform of possible deviations occurred during the process of Quality inspection.
To ensure that all tasks are performed in a timely manner.

**Academic experience required**
Bachelor ‘s Degree in Health-related Sciences.
Knowledge of cGMP requirements preferred

**Professional experience required**
Preferably at least 2 years of experience in a similar position, in environments of Good
Manufacturing Practices (GMP) in Pharmaceutical background.

**Computing skills**
MS Office knowledge.
SAP experience, preferable.

**Personal skills**
Organized and able to manage time effectively.
Ability to work within a highly regulated, labor intensive environment.
Ability to understand, explain, follow, and enforce SOPs.
Ability to plan, communicate and execute activities for the improvement of overall operations.
Strong integrity and commitment to Quality and Compliance.
Ability to work in groups and with other departments.
Excellent oral and written communication skills to produce clear and concise factual findings.
Ability to identify problems and propose solutions.

**Languages**
Written and spoken English and Arabic.

LI-MB1

Third Party Agency and Recruiter Notice:
**Grifols provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other characteristic or status protected by law.** We will consider for employment all qualified Applicants, including those with Criminal Histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance.**

**Location**:EMEA : Egypt : Egypt**:EGTOLIP - Tolip El Narges-New Cairo**

Learn more about Grifols



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