Center Quality Specialist - Banha at GRIFOLS, S.A.

Banha, Al Qalyubiya, Egypt -

Full Time

Start Date

Immediate

Expiry Date

26 Sep, 26

Salary

0.0

Posted On

28 Jun, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Assurance, cGMP, SOP Editing, Quality Management, Document Review, Equipment Quality Control, Compliance, MS Office, Organizational Skills, Attention To Detail, Problem Solving, English Proficiency, Arabic Proficiency

Industry

Pharmaceutical Manufacturing

Description

Job Description 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 SOPs related to processes at donor center level following the guidelines established according to Egyptian regulations and the guidelines established according to cGMP requirements. 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 SOPs are followed. To assist to CQM in the edition of SOPs. To perform a review of the documentation of unsuitable test results and the disposition of the associated units Job Requirements Bachelors Degree in Health-related Sciences. Knowledge in Quality Management Strong integrity and commitment to quality and compliance Preferably at least 2 years of experience in a similar position, in environments of Good Manufacturing Practices (GMP) and Pharma background. MS Office knowledge 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. Written and spoken English and Arabic.

Responsibilities

Perform quality assurance functions to ensure compliance with internal and external regulations and cGMP requirements. Responsibilities include reviewing donor center records, editing SOPs, and inspecting incoming supplies and sample shipments.