Validation Engineer (32019j)
Validation Engineer -Support the activities of Operations / Engineering / Information Management in assuring compliance with the pertinent regulations. JobTitle. Validation Engineer. About CompanyOur client based in Limerick is seeking a Validation Engineer to join its expanding team. Duration of Role18 Months. Summary ObjectiveDevelop Validation Documentation to support new process/product introductions and existing business continuity and process improvement requirements. Job 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 introductions - Implementation and co-ordination of the change control process, promotes timely approval of all supporting documentation - All employees are responsible for minimising both the Environmental and Health & Safety effects of the work that they perform. Requirements. Skills & ExperienceEssential: - Bachelors degree from accredited college - 3/5 yrs in a Quality function within the Medical Device/ Pharmaceutical industry. - Have good knowledge of statistical techniques in the use of problem solving/ data analysis. - Have a proven track record in development/execution of Validation programs in areas of Equipment, Process Information management - Ability to demonstrate standards of leadership – Managing Complexity/Credo Values/Innovations/Customer focus. - Flexible - Team Player - Good Influencing Skills - Project Management Skills - Good generalist - Good communication skills - Methological Desirable: - Be very familiar with the relevant regulatory standards (F.D.A. - Quality System regulations, IS 13485) applicable to the manufacture of Class 111 medical devices to Global markets. BenefitsBenefits of workingwith Independent Solutions. > Excellent Team of Colleagues. > Accessto high-value projects. >Excellent Technical Project Managers. > Excellent pay &conditions. At Independent Solutions, we will notrequire you to become an employee of Independent Solutions, we will facilitateand support you to become an independent contractor, thereby reaping themaximum rewards from your contract role. Yes, of course we benefit fromhaving YOU with US, but we can assure YOU that YOU too will benefit … This job originally appeared on RecruitIreland.com.
67 days ago