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Job Description
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.
- 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)
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