senior developer
Tabuk pharmaceutical research&development
Total years of experience :17 years, 3 Months
- Analytical Test procedure development
-Data checking and method compliance
-Trainer of employee
-Technical support for colleagues
-Instruments and software troubleshooting
Being an effective part of the action plans as a part of QC preparations to receive the external audits. Such as FDA and the MHRA audits.
Follow up the application of cGMP’s & cGLP’s in QC labs.
Training new section employees on working in the laboratory and good documentation practice.
Follow up and implementing FDA and MHRA recommendations for industry.
Joining a two months practical course at Hikma Pharmaceutical - Chemicals Plant(June-August 2006)