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 effectivenessWork with the various departments/groups in development and execution of validation activities associated with new equipment/product or I.M.
system upgradesRuns /Manages complaint investigation and resolution of sameDesigns and develops validation documentation to support business continuity, new process/product introductions and process improvement requirementsImplementation and co-ordination of the change control process promotes timely approval of all supporting documentationImplement policies and proceduresAll 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 effectivenessWork with the various departments/groups in development and execution of validation activities associated with new equipment/product or I.M.
system upgradesRuns /Manages complaint investigation and resolution of sameDesigns and develops validation documentation to support business continuity, new process/product introductions and process improvement requirementsImplementation and co-ordination of the change control process promotes timely approval of all supporting documentationImplement policies and proceduresAll employees are responsible for minimising both the Environmental and Health & Safety effects of the work that they perform. Experience and Education: A Bachelor's degree2-3 years in a Quality function within the Medical Device/ Pharmaceutical industryBe 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 ****** for further information.
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