Category
Quality
Publish Date
Sunday 24-08-2025
Country
Egypt
Gender
any
Years Of Experience
10-15 Years
Salary
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.
