Quality Validation Engineer
SMC6706
Contract - 12 months
Limerick
We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Limerick. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.
Duties:
* Responsible for supporting the activities of Operations / Engineering / Information Management in building product Quality into our products and assuring compliance to the pertinent regulations while at the same time attaining operational effectiveness
* Work with the various departments/groups in development and execution of validation activities associated with new equipment/product or I.M. system upgrades
* Runs /Manages complaint investigation and resolution of same
* Designs and develops validation documentation to support business continuity, new process/product introductions and process improvement requirements
* Implementation and co-ordination of the change control process promotes timely approval of all supporting documentation
* Implement policies and procedures
* All employees are responsible for minimising both the Environmental and Health & Safety effects of the work that they perform.
Quality Validation Engineer
SMC6706
Contract - 12 months
Limerick
We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Limerick. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.
Duties:
* Responsible for supporting the activities of Operations / Engineering / Information Management in building product Quality into our products and assuring compliance to the pertinent regulations while at the same time attaining operational effectiveness
* Work with the various departments/groups in development and execution of validation activities associated with new equipment/product or I.M. system upgrades
* Runs /Manages complaint investigation and resolution of same
* Designs and develops validation documentation to support business continuity, new process/product introductions and process improvement requirements
* Implementation and co-ordination of the change control process promotes timely approval of all supporting documentation
* Implement policies and procedures
* All employees are responsible for minimising both the Environmental and Health & Safety effects of the work that they perform.
Experience and Education:
* A Bachelor’s degree
* 2-3 years in a Quality function within the Medical Device/ Pharmaceutical industry
* Be very familiar with the relevant regulatory standards (F.D.A. - Quality System regulations, ISO 13485)
If interested in this posting please feel free to contact Sean McCarthy on +353 087 798 8480 or sean.mccarthy@lifescience.ie for further information.
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