What you will do
You will have a great opportunity to learn more about pharmaceutical development working with experienced operators. This role contributes to the manufacturing of drug products in development phase for clinical studies. All below activities will have an impact on the speed, quality and cost of the AZ development portfolio.
As part of the EPDM manufacturing unit, your work will focus on the manufacturing of drug product. You will perform practical hands-on work in our Good Manufacturing Practice (GMP) facilities with dedicated tasks in close collaboration and to support EPDM Scientist/Senior Scientist e.g. assisting GMP operators with:
• Preparation of process rooms before and after clinical manufacture
• Assembly/disassembly and cleaning of equipment
• Dispensing of API (Active Pharmaceutical Ingredients) and excipients (inactive pharmaceutical ingredients)
• Bulk packing
• Visual inspection of drug products
• Metal check of drug products
• Check of log books
• Working according to SHE (Safety Health and environment) and GMP standards
The role is intended to be used in a flexible way to resolve short term bottle necks. The role holder will not become fully qualified as a GMP operator but will be able to carry out much of the work expected from operators under supervision.
Does this sound like your next challenge? Apply today! Deadline 2025-01-23 - the selection process and interviews will be ongoing, so please apply as soon as possible!
For more information: Please contact Katan Ali, katan.ali@randstad.se. Please note that applications sent through email will not be processed and deleted due to GDPR.
