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Job Description
- Follows all relevant Quality policies, processes and standard operating procedures so that work is carried out in a controlled and consistent manner.
- Implements the day-to-day operations assigned for the function to ensure compliance with the established standards and procedures.
- Supervises the day to day operations of quality departments related to one providing some guidance in facilitating related professional work processes in order to achieve high performance standard
- Conducts and operates inspections and quality plans in the different areas.
- Maintains standards by reviewing, checking and monitoring work output to ensure quality requirements are met.
- Deals with external contacts such as clients and engineers and resolves non-routine queries and problems or refers as appropriate.
- Disseminates and escalates quality communications appropriately across the business units.
- Provides individual and team information on quality issues in the form of reports/statistics to support decision-making and reporting at a higher level.
- Prepare complex reports to be submitted to the concerned departments or managers.
- Prepare standard operation procedures (SOPs) for quality processes according to cGMP’s guidelines
- Trains lower-level jobs on tasks to ensure compliance with set cGMP’s guidelines and SOPs.
- Complies with all relevant safety, quality, health and environmental procedures to ensure a healthy and safe work environment.
Job Requirements
- BSc. In Pharmacy or Science
- with minimum 5 years experience in validation activities in Sterile manufacturing. Validation activities (Media fill & Cleaning Validation, beside normal Validation activities).
- Preferably (Cairo, Obour, New Cairo, Nasr City, Heliopolis, Badr, Zagazig, Sharqia, and 10th of Ramadan) residents.
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