Job Category: QA/QC Engineer
DOX Pharma
Any related speciality with max two year experience or fresh graduate
Only Saudi or whom inside Saudi Arabia can apply
Immediate joining will be an advantage
Responsibilities
1.Control all the departments documents from distribution, keeping and archiving.
2.Follow up the production and packaging process with the batch record as per cGMP such as (line clearance , in
process control and sampling).
3.Ensure the implementation the training plans for the employees.
4.Participate and involved in the internal and external audit.
5.Perform daily check on the different sections in the company.
6.Participate and involved in the process and cleaning validation.
7. Review the manufacturing and Packaging batch record.