Do you want to join an international team working to improve the future of
healthcare? Do you want to improve the lives of millions of people? Grifols is
a global healthcare company which, since its foundation in Barcelona in ‎1909,
has been working to improve the health and well-being of people all over the
world. Our four divisions - Bioscience, Diagnostic, Hospital and Bio Supplies
- develop, produce and market innovative medicines, solutions and services in
more than ‎100 countries and regions.

JOB OBJECTIVE
To ensure the correct implementation of Standard Operating Procedures (SOP 's)
in plasma center following the guidelines established
To evaluate processes, develop action plans, and coordinate the strategic
implementation of system
processes and corrective actions in order to ensure product quality, donor
suitability and donor safety.

ENVIRONMENT
Internal: Manufacturing, Quality global, Supply Chain, Administration &
Services divisions, and Grifols Egypt for Plasma Derivatives plasma general
management.
External: donors, Health Authorities, groups, business service providers,
auditors, and community and neighborhood organizations.

KEY RESPONSIBILITIES
* To direct and monitor processes and to ensure DC compliance with Egyptian Regulations and company- designated regulations.
* To collaborate with Center Manager to ensure product quality, donor suitability and donor safety.
* To ensure that SOPs are properly interpreted, implemented in a timely fashion, and that the staff performs according to all SOPs.
* To interpret and implement processes, regulations and SOPs for quality control and overall regulatory compliance, making independent decisions and modifications as required.
* Oversight of all aspects of internal and external audits including execution (if applicable). This includes documentation, review of and preparation of the response.
* Continuously assesses, promotes, and improves the effectiveness of the quality systems in the DC through recognition of trends, investigation of failures in the execution of procedures, direct employee observation and review of center documents.
* Responsible for the personnel functions of the Quality Plasma center Specialist(s)
* Oversees product and biohazard waste shipments: Ensures shipments meet regulatory specifications and product release requirements; ensures accurate labeling and documentation; and, authorizes final shipment.
* To perform a review of the documentation of unsuitable test results and the disposition of the associated results.
* To document, investigate, and perform root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.
* Ensures that job and Current Good Manufacturing Practice (cGMP) training is completed, documented, and on file.
* Partners with the Center Manager to determine donor suitability activities and manages donor deferrals as appropriate
* Reviews and approves of deferred donor reinstatement activities
* Performs a review of lookback information
* Reporting center quality status to plasma QA senior Manager to provide additional oversight and guidance.
* Tracks/Trends and performs follow-up on corrective and preventative actions, system implementations, and process improvement plans to measure/determine effectiveness. Makes adjustments where required

ACADEMIC EXPERIENCE REQUIRED
B.S. degree, preferably in a health-related science.
Preferably Post- Graduate Certification in Quality Management

PROFESSIONAL EXPERIENCE REQUIRED
‎2 years of Experience on Quality system tasks desired . Supervisory experience
preferred. Experience in a medical and/or cGMP regulated environment
preferred. Experience with plasma or whole blood preferred.

COMPUTING SKILLS
Proficiency in Computers

PERSONAL SKILLS
* Ability to understand and assess relevant regulations.
* Ability to understand, explain, follow and enforce SOPs, protocols and other regulatory guidelines.
* Proficient in root cause analysis and corrective/preventative actions
* Ability to balance multiple competing priorities
* Strong time management abilities
* Ability to work with minimal supervision
* Accuracy and reliability.
* Ability to work in groups and with other departments.
* Adherence to the Grifols skills and values.

LANGUAGES
Written and spoken English and Arabic

LI-LS1

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

Learn more about Grifols