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
To define and organize the Plasma Testing Laboratory, in compliance to
Egyptian regulations, and in accordance to cGMP, following Plasma Testing
Specifications established and European Regulation. To manage plasma testing
laboratory resources, optimizing the assigned resources to test plasma samples
received to comply with the agreed planning and to guarantee plasma quality
and safety.

Environment
Internal: Donor Center Managers, Procurement & logistics department, facility
& engineering department, General Services Manager, Epidemiology Manager,
Plasma QA Senior Manager, QC Plasma Sr Manager, QC testing Specialist and QA
Specialist.
External: Health Authorities, Government authorities and auditors.

Key responsibility
Plasma Quality Control:
* To train, supervise and support specialists to ensure tasks are performed correctly
* Able to Schedule staff and to improve their productivity and efficiency and that lab time is allocated adequately.
* Monitoring quality control to ensure that all Plasma testing results are accurate.
* Ensure samples are handled correctly and that all safety procedures are followed in the lab.
* To follow all Plasma testing laboratory procedures and processes.
* To monitor the laboratory inventory and ensure that all materials are ordered and in place.
* To initiate and improve laboratory documents and reports.
* Creating reports with data analysis of findings related to laboratory activities and documents.
* Ensure the calibration program for the Laboratory equipment is performed as planned.
* Facilitate effective communication across internal departments by trending and reporting data.
* To participate and support Regulatory inspections and audits run in the Lab.
* Ensure adherence to regulatory requirements, budgets, and schedules.
Academic experience required
* Scientific Degree in pharmaceutical or biomedical area preferred.
* Preferably master's degree in Clinical Pathology or transfusion medicine Laboratory.

Professional experience required
* Minimum ‎8 years of experience in certified laboratories
* Minimum ‎3 years of experience in a similar position, in environments of Good Manufacturing Practices GMP.
* Knowledge in Good Laboratory Practices (GLP's).

Computing skills
* Proficiency in Computers.

Personal skills
* Excellent communication skills, verbal & written.
* Agility to learn & study in a fast-paced environment.
* Accuracy and reliability.
* Able to identify problems, root cause, & propose solutions
* Excellent time management & planning skills.
* Leadership and managing diversities.

Languages
* Fluent English and Arabic language.

LI-LS1

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

Learn more about Grifols