Search Results: 8 vacancies
...knowledge of aseptic Drug Product manufacturing processes; Parts/Components Preparation Formulation Syringe Filling Vial Filling Lyophilisation and Capping.
As a Process Owner Lead you will be an established professional who is a selfstarter capable of applying advanced...
...:
• Typically 4-6 years drug product experience in areas such as drug product formulation, vial/pre-filled syringe filling or lyophilisation
• Qualification in Lean and 6-sigma methodologies would be an advantage.
• New product introduction (NPI), process development...
€ 50 - 60 per hour
...Engineer/Scientist with 5+ years drug product experience in areas such as drug product formulation, vial/pre-filled syringe filling or lyophilisation ? The is a contract role based on site in Dun Laoghaire, Dublin.
If you have the relevant experience, please forward your CV to...
...analytical development, product development including verification and validation using LC-MS/MS technology, manufacturing including lyophilisation, quality control and on-market support.
The successful candidate will:
Transfer manufacturing processes from...
...knowledge of aseptic Drug Product manufacturing processes; Parts/Components Preparation Formulation Syringe Filling Vial Filling Lyophilisation and Capping.
The Site Aseptic Process Lead will continue to build on the site and network aseptic processing knowledge....
...executingtechnical projects supporting Drug Product manufacturing within Formulation,Component Preparation, Vial/Syringe Filling, Lyophilisation, Device Assembly,Inspection, Labelling and Packaging areas. This includes qualification of newequipment and implementation of associated...
...Operations at the Dun Laoghaire site in Dublin, Ireland, key and expanding site in Amgen’s global manufacturing network and Amgen’s global Lyophilisation centre of excellence.
Business Resilience Manager
Live
What you will do
Let’s do this! Let’s change the world! In this...
...etc.)
· Providing technical interpretation and guidance of current US FDA and EU validation requirements for aseptic processing, lyophilisation, sterilisation and depyrogenation
· Ensuring that the validation status of equipment and systems are in compliance with cGMP at...