Job Scope
Monitor the product process, control the quality of the products and insure accurate application of GMP rules in
every step of production.
Job Requirements
- At least B.Sc. or Diploma in Pharmacy, Chemical Engineering, Industrial Engineering, or Science.
- One year of relevant experience.
- Good written, read and spoken Arabic and English Languages.
Professional Knowledge
- Knowledge in the systems such as ICH, GMP, GLP, WHO.
- Knowledge in production area layout design.
- Knowledge in Trend Analysis
- Failure investigation.
- Knowledge in material, process and people flow.
- Statistical Analysis.
- Systems development & workflow.
Main Competencies
- % of defects/ violations/ deviations found on Process control.
- Average number of quality checks vs. target.
- % of deviation reports approved vs. generated.
- % of action points derived from internal-audit, implemented within time planned.
- Number of units rejected by quality inspection
- Number of customer complaint due to quality of services
- Effectiveness of Process Audits
Duties And Responsibilities (But Not Limited To)
- Ensure implementation of GMP rules in production area and to control those related to employee practices
- such as gowning in production area and prevent presence of contamination sources such as food and drink.
- Checking general cleaning in production area.
- Controlling calibration of the instruments in IPC section according to the relevant SOP.
- Comparing each identification card of every room with the product inside.
- Ensure the safety of production process
- Line clearance in all areas in production
- Sampling: Sampling of bulk and finished products.
- Patches: weight, weight variation, sealing, appearance & printing.
- Checking the over printing on boxes, labels recording to the production order
- Checking inspection during production
- Keeping the rejected products in reject stage to destruction
