Category QualityPublish Date Sunday 24-08-2025Country EgyptGender anyYears Of Experience 10-15 YearsSalary Negotiable“QA Manager” is required for a multinational healthcare company located in New Cairo.Responsibilities:
Providing QA support for assigned TPMs to ensure that safe, efficacious, and quality product can be supplied to meet cGMP and other applicable regulatory standards and the appropriate market requirements.
Responsible for development of Quality Improvement Plan for TPMs remediations, when required.
Responsible for Monitoring quality performance for assigned TPMs, and ensure requirements per Quality Technical Agreements are adhered and followed by assigned TPMs.
QA Lead for investigations, trends, complaints, corrective and preventive actions (CAPA), validation support, product release issues, PQR review and change control at TPM sites
QA lead for co-ordination with TPMs and internal cross functional team as support and interfaces for routine Quality requirements like GMP audits, new projects or initiatives.
Responsible for maintaining regional Approved TPM Listing.
Responsible for communication with Global TPM QA regarding Global TPM Products that are supplied for Egypt, part ofEMEA region.
Responsible for supporting Global and Regional Quality Compliance and improvement initiatives.
Support new contract manufacturing site approvals within responsibility in Egypt.
Requirements:
Bachelor’s degree in science, Pharmacy or equivalent level of education at a relevant scientific discipline.
Minimum 10+ years of experience in the pharmaceutical manufacturing field (Quality, production, technical support,etc).
Comprehensive understanding of a wide range of Pharmaceutical Manufacturing and Testing Operations.
Knowledge of international and local quality system and compliance legislations and standards.
GMP/GLP/GCP background related to medicinal products, medical device, food supplement Biotechnological, Biosimilars and Biologics.
