Validation Engineer required for a leading medical device company based in Limerick. The companies FDA regulated Limerick facility has grown consistently over the last 20 years to become one of the most important sites in its global operations. This facility specialises in the production of disposable contact lenses in a state of the art operation which includes injection moulding, robotics, vision systems and sterilisation systems in a Class 100,000 cleanroom environment. The facility has over 50 fully automated manufacturing lines and the product is untouched by a human hand from start to finish of the process.
If you are looking for an opportunity to work in a leading edge medical device facility with a focus on process innovation, automation and continuous improvement with steady personal growth and development opportunities then call us to find out more.
Excellent opportunity for a Validation Engineer with responsibility for ensuring:
o The support the activities of Operations / Engineering / Information Management in assuring compliance with the pertinent regulations
o Work with all departments in ensuring operational effectiveness and developing product Quality for business continuity and process/product introductions.
In this role the Validation Engineer will:
o Be 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
o Work with the various departments/groups in development and execution of validation activities associated with new equipment/product or I.M. system upgrades
o Runs /Manages complaint investigation and resolution of same
The Validation Engineer requires:
o Bachelors degree from accredited college
o 3/5 yrs in a Quality function within the Medical Device/ Pharmaceutical industry.
o Have good knowledge of statistical techniques in the use of problem solving/ data analysis.
o Have a proven track record in development/execution of Validation programs in areas of Equipment, Process Information management
If this role is of interest, please call Martin at LSC on 021 4777 329 or apply directly through this advert