- Promote conformance to GMP's and FDA regulations.
- Evaluate addressed deficiencies for potential impact on compliance status while working with all concerned departments to correct any noted deficiencies/inconsistencies.
- Ensure compliance with current Good Manufacturing Practices (cGMP), Company Standard Operating Procedures (SOPs), and authority regulations and guidelines.
- Ensure compliance with all Company policies and procedures, including safety rules and regulations.
- Follow up balances calibration
- Follow up quality of finished product by inspection in time intervals
- Proper application of line clearance from the previous products.
- Perform checking conformance to G.M.P& FDA regulation (room temperature-Magnehelic reading - humidity– Cleaning concept).
- Monitor the environment of production areas.
- Ensure calibration and validity calibration for balances.
- Ensure the presence of the batch record which indicate the whole history for products
- Record every CPP & CQA of finished product and reporting of unusual incidents.
- Revising inkjet and embossing data.
- Make sure of welding of the tube and occurrence of burst test for tubes.
- Make sure of presence of all SOPs related to the production area (machines- gowning- washing process- personal hygiene – personal knowledge for workers)
- Revising all produced batches on production lines.
- Reviewing the bulk product barrels to be sure from its conformity with the reference samples.
- Make sure of presence of reference standard sample to be weighed.
- Make sure from the conformity of the finished product with the reference sample (Product name- conform design – printed data – primary and secondary pack- color- homogeneity- odor).
- Attending all new products trials in production areas.
- Observe conditions on line and in-process area for compliance with the process method for correct operation of procedures and for cleanliness and clearance of other components.
- Ensure of recording all deviation and out of control cases which related to the production areas.
- Revising and checking reference samples of finished products for each batch to obtain representative samples, which conform to standard samples from 1st, 2nd and 3rd of line.
- Examine the supplier defect before returning to the warehouse.
- Contact with concerned department when there’s problem with bulk or packaging material.
- Ensure the implementation of HSE regulation.
BSc in Science or Pharmacy.Quality assurance experiences is must.Personal Care products experience is preferred.Ability to work overnight.Accountable and team player.