- Preparing of QA department SOPs & procedures.
- Writing official documents concerning QA in coordination with QA Head.
- Preparing management review agenda, writing meeting minutes and final report.
- Follow up of QMS requirements in all departments (quality objectives – KPIs – customer satisfaction...etc).
- Issue, maintain and writing SOPs concerning QA department or other departments based on the latest updated references.
- Review & Issue specifications, Test methods of analysis, MFPIs, protocols and plans & its update.
- Issue site master file & quality management system manual.
- Review packaging material art work and issue master packaging file.
- Issuance & updating and control of master batch records.
- Collect Annual product review data & Prepare Annual product review report.
- Responsible for making statistical analysis for Annual product review.
- Ensure IPCs inside the factory.
- Issuance & Updating batch manufacturing records & batch packaging records.
B.Sc. of Pharmacy or science.Not less than 3 years of experience in a similar position.Good understanding of the rules and guidance of GMP and GDP.Good English language.Professional using Microsoft office.Excellent communication skills.integrity and professional ethics.Attention to detail.