Center Quality Assurance Specialist (EGYPT) - Port Said

؜ - ؜مصر ؜ -

Job details

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 perform Quality Assurance functions to ensure compliance with internal and external regulations and 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 cGMP requirements.

ENVIRONMENT

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 RESPONSIBILITIES

* 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.
* 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.


LI-LS1


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


Learn more about Grifols

Job Summary

  • Advertiser: Grifols
  • Announcement date: 24/02/2023
  • Type of employment: -
  • Experience level: -
  • Educational level: -
  • Salary: -
  • Phone number: -

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