QC Methodology Section head

• Development of analytical procedures for drug products under development.
• Validation of the developed analytical procedures according to ICH guidelines.
• Handling troubleshoots during product development.
• Periodical review of developed analytical methods. 
• Respond to relevant requirements of the registration & export departments. 
• Capable in managing, training, and coaching staff to achieve the lab KPIs.

Ensures that all activities in his unit or section are done according the relevant cGMP and ISO standards (ISO 9001, ISO 14001, OHSAS 18001).

• PhD or M.Sc. in pharmaceutical sciences. Or relevant degree.
• Suitable training relevant for the job
• Analytical thinking, problem solving and communication skills.