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Job Description
- Design, implement and improve QC systems including Method Validation, Documentation system, testing procedures and compliance.
- Ensure implementation of data integrity program within QC and on-site operations level.
- Preparation of monthly quality metrics to follow-up the performance of quality functions.
- Preparation for quality-related audits (Internal or External).
- Ensure that all activities and processes are operate and comply with GLP regulations and specific regulations of vaccine industry.
- Supervises staff and oversees product development procedures to ensure that products meet quality and efficiency standards.
- Supports activities related to analytical method transfer for the assigned projects to ensure efficient transfer of projects technology.
- Keeping Quality Control protocols, method and practices updated and matched with related references.
- Manage department budget and responsible for implement cost saving
Job Requirements
- Bachelor's Degree Pharmacy or Science.
- Pharmaceutical Industry experience is a must.
- +15 years of Experience in QC and sterile Product (at least 5 years of progressive managerial level).
- TQM, Six Sigma, ISO 17025 Certified is preferred.
- Charismatic, presentable, communication Skills, analytical thinking and Decision Maker.
- GIZA residence preferred.