Center Quality Assurance

Grifols Egypt for Plasma Derivatives; Egypt (PA); On-site; USD 12,000 - 18,000; Full time

Job summary

Grifols Egypt for Plasma Derivatives is seeking a Quality Assurance QA Specialist to support and maintain quality systems ensuring compliance with internal procedures and regulatory requirements.

The role requires a Bachelor’s in health-related sciences (pharmacy preferred), at least 2 years GMP experience in pharma quality, strong documentation discipline, and proficiency in MS Office to support cross-functional teams and uphold SOPs and cGMP standards.

Qualifications

• Bachelor's degree in health-related sciences; pharmacy preferred; knowledge in quality management.
• At least 2 years of GMP experience in pharma quality.
• Proficient in MS Office; strong documentation and regulatory compliance.

Responsibilities

• Ensure SOPs and cGMP regulations are followed
• To perform periodical review of DC GMP related records
• To perform periodical equipment quality control review
• To perform periodical review of equipment incident logs
• To verify and release sample shipments
• To inspect and release incoming supplies
• To perform periodical employee observations

Skills

SOPs & cGMP

Quality Assurance

Education

Bachelor's Degree in Health-related Sciences (Pharmacy preferred)

Tools

Ms Office

Job description

The Quality Assurance QA Specialist is responsible for supporting and maintaining quality systems to ensure products and processes comply with internal procedures as well as local and international regulatory requirements

• Key responsibility Ensure SOPs and cGMP regulations are followed
• To perform periodical review of DC GMP related records
• To perform periodical equipment quality control review
• To perform periodical review of equipment incident logs
• To verify and release sample shipments
• To inspect and release incoming supplies
• To perform periodical employee observations

Academic experience required

• Bachelor's Degree in Health-related Sciences. Preferably in Pharmacy. Knowledge in Quality Management. Strong integrity and commitment to quality and compliance.

Professional Experience Required

• At least 2 years of experience in Good Manufacturing Practices (GMP) environments in Quality Area within Pharma industry.

Computing Skills

• Ms Office knowledge.

Personal Skills

• Ability to understand, explain, follow and enforce SOPs, protocols and other regulatory guidelines. Accuracy and reliability. Can work independently, excellent organizational skills, and attention to detail. Performs a high-level document review. Ability to work with cross functional areas. Good ability to identify problems and propose solutions.

Languages

• Intermediate level of written and spoken English Fluent in Arabic.