QA Officer

Job Category:

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.

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