• Supervising all section activities, including attendance and proper use of equipment.
  
• Ensuring section production plans/programs are implemented and strictly followed.
• Coordinating section production activities with the Quality Assurance department and other sections of Production, and preparing     daily section shifts and monthly reports
• Fully enforcing the cGMP throughout the section, including cGMP training.
  
• Planning and controlling section requirements for consumables and accounting for materials.
  
• Ensuring safety/hygiene of personnel, equipment/facilities, drug material, and all documents/records in the Section.
  
• Documenting all events that lead to the machine/activity breakdown.
• Any other duty assigned from time to time by your Head of Department.

Academic Qualifications

Bachelor’s degree in Pharmacy, Industrial Chemistry, Chemical Engineering, or a related field

How to Apply:

All applications will be received and reviewed through the BrighterMonday Portal by clicking on the 'Apply Here' section