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Validation Engineer Limerick Contract
Eingestellt von Computer People
Gesuchte Skills: Engineer, Design
Projektbeschreibung
Senior Software/Computer QA Validation engineer - Ireland/Limerick
My client a leading player with the Limerick area is in urgent need of a talented and experienced QA Validation engineer to join them on a permanent basis. You will be required to Co-ordination, implementation and actively participate in the validation programme for all business computer systems. You will be looking to lead small team of computer validation specialists.
Candidates will conduct validation activities in compliance with US and EU regulations, and global corporate procedures. You will also be required to provide input into all project phases ie from design through to the commissioning and qualification execution phases of the project. It will be mandatory that candidates are able to develop validation documentation as required; You will also look to review and approve documents prepared by the validation team, other functional departments and contractors.
You will have a minimum of 5 years IT validation experience in an established QA function in the Pharma industry and have a strong knowledge of CSV/GAMP, 21CFR Part 11, Project Life Cycle and GMP Regulations Validation experience of GAMP 5 systems would be an advantage
This is a great role to get into with a firm that is looking to expand; drop me your CV today or a line if you would like to discuss in more detail.
My client a leading player with the Limerick area is in urgent need of a talented and experienced QA Validation engineer to join them on a permanent basis. You will be required to Co-ordination, implementation and actively participate in the validation programme for all business computer systems. You will be looking to lead small team of computer validation specialists.
Candidates will conduct validation activities in compliance with US and EU regulations, and global corporate procedures. You will also be required to provide input into all project phases ie from design through to the commissioning and qualification execution phases of the project. It will be mandatory that candidates are able to develop validation documentation as required; You will also look to review and approve documents prepared by the validation team, other functional departments and contractors.
You will have a minimum of 5 years IT validation experience in an established QA function in the Pharma industry and have a strong knowledge of CSV/GAMP, 21CFR Part 11, Project Life Cycle and GMP Regulations Validation experience of GAMP 5 systems would be an advantage
This is a great role to get into with a firm that is looking to expand; drop me your CV today or a line if you would like to discuss in more detail.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Ingenieurwesen/Technik