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Project Engineer C&Q
Eingestellt von Quanta Consultancy Services
Gesuchte Skills: Design, Engineer
Projektbeschreibung
Role: Project Engineer C&Q
Type - initially 12 month contract
Location - Co. Cork
Key Responsibilities
Person will act as a system owner through design, field installation, drafting of C&Q protocols based on site standard and be involved with commissioning with the vendor and will be required to handover the system to end user with suitable documentation etc
Vendor management of a vendor company based in Italy.
Will involve co-ordination/transfer of information to other disciplines as part of overall design.
There are two cappers that are purchased and integration within the facility is by two different design houses and the successful candidate will be required to interface with both.
Will involve short term international travel to FATs (1-2 weeks) and for design reviews as required.
Involve co-ordination of feedback from end users and ensuring design meets the needs of the business
Key Requirements
Strong experience within a pharmaceutical environment is a must, preferably within a sterile environment is strongly preferred
Experience in writing and execution of C&Q protocols, conducting FATs and regular liaison with the vendors and suppliers
Experience and knowledge of any capping/vision/vial handling equipment is a preference.
Type - initially 12 month contract
Location - Co. Cork
Key Responsibilities
Person will act as a system owner through design, field installation, drafting of C&Q protocols based on site standard and be involved with commissioning with the vendor and will be required to handover the system to end user with suitable documentation etc
Vendor management of a vendor company based in Italy.
Will involve co-ordination/transfer of information to other disciplines as part of overall design.
There are two cappers that are purchased and integration within the facility is by two different design houses and the successful candidate will be required to interface with both.
Will involve short term international travel to FATs (1-2 weeks) and for design reviews as required.
Involve co-ordination of feedback from end users and ensuring design meets the needs of the business
Key Requirements
Strong experience within a pharmaceutical environment is a must, preferably within a sterile environment is strongly preferred
Experience in writing and execution of C&Q protocols, conducting FATs and regular liaison with the vendors and suppliers
Experience and knowledge of any capping/vision/vial handling equipment is a preference.
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Medien/Design, Ingenieurwesen/Technik