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Autoclave Validation Engineer
Eingestellt von Quanta Consultancy Services
Gesuchte Skills: Engineer, Engineering, Support
Projektbeschreibung
Working for a Global Pharmaceutical organisation who currently requires an experienced Autoclave Validation Engineer to work at their sterile manufacturing facility in Carlow, Ireland.
This role will be part of the Technical Operations Validation team starting up, validating and providing on going technical support to the filling processes at our Vaccines Formulation/Fill facility in Carlow
Key Responsibilities:
To actively participate in heat penetration/distribution studies associated with cycle development and PQ using Kaye thermal system and biological challenges.
Participation in the drafting and reviewing of validation documentation and procedures.
Accountable for the execution, completion and tracking of validation documentation to a required standard.
Actively contribute to project teams.
Key Experience:
Validation experience in vaccine or sterile product manufacturing would be an advantage (min 3 - 5 years)
Thermal mapping experience using Kaye systems
Experience in IMB/FDA environment advantageous.
Strong technical writing and communication skills
Must be goal-oriented and able to manage risks.
Project management skills
Education:
Degree level qualification in Science or Engineering
This is an excellent opportunity to work for a dynamic, ever growing organisation. Please contact me for further details.
This role will be part of the Technical Operations Validation team starting up, validating and providing on going technical support to the filling processes at our Vaccines Formulation/Fill facility in Carlow
Key Responsibilities:
To actively participate in heat penetration/distribution studies associated with cycle development and PQ using Kaye thermal system and biological challenges.
Participation in the drafting and reviewing of validation documentation and procedures.
Accountable for the execution, completion and tracking of validation documentation to a required standard.
Actively contribute to project teams.
Key Experience:
Validation experience in vaccine or sterile product manufacturing would be an advantage (min 3 - 5 years)
Thermal mapping experience using Kaye systems
Experience in IMB/FDA environment advantageous.
Strong technical writing and communication skills
Must be goal-oriented and able to manage risks.
Project management skills
Education:
Degree level qualification in Science or Engineering
This is an excellent opportunity to work for a dynamic, ever growing organisation. Please contact me for further details.
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Ingenieurwesen/Technik, Sonstiges