Center Quality Assurance Specialist - Tanta
Grifols Egypt for Plasma Derivatives · Tanta, Tanta, Egypt ·
- Category
- QA
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.
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.
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.