Category

Description

• Control Quality analysis by HPLC; GC, UV, Dissolution test, ph, espectophotometry, and others.
• Stability studies
• Analytical troubleshooting
• Data review to the relevant regulatory standard, analytical procedures and appropriate documentation
• Laboratory reports and investigation reports
• Updating documentation when required

Requirements

• Degree in chemical sciences or related disciplines.
• 1 years laboratory experience in similar position in the pharmaceutical or related industry.
• Essential 1 years analytical experience using HPLC /GC
• Experience in studies of stabilities, sample management and analysis.
• PNT Writing
• Knowledge of GMP/GLP environment
• Used to work as a team and focused on goals.
• High level of English
• Passionate about quality and customer service
• Good communication skills both internally and exernally

It Is Offered

• To be a part of a motivated and active group.
• Full time Permanent Position.