Description
I am currently working with a multinational biopharmaceutical company who is looking for a Senior Quality Control (QC) Associate to join their team. You will be working on a 12 month contract in Dun Laoghaire, Ireland.As a Senior QC Associate, you will be responsible for authoring Validation Life Cycle documents for laboratory computer related systems, also responsible for executing and documenting the qualification and ensuring the integrity of data in the validated system, calibration and routine maintenance of laboratory systems for cGMP Quality Control laboratory facilities.
Your key skills / experience will include:
> Minimum of BSc in a (Biological) Sciences related discipline
> Minimum of 3 years' experience in a cGMP environment executing instrument validation and managing Laboratory Computer Related System Validation Lifecycle > Good understanding of Windows® Operating Systems and proven experience of troubleshooting issues identified during laboratory systems validation
> Experience of authoring and executing cGMP Validation documents in a controlled document system
>Experience of resolving Protocol Deviations and Root Cause Analysis
>Awareness of Change Control philosophy in the cGMP environment
>Understanding of current regulatory requirements for cGMP laboratory equipment validation and electronic record / electronic signature integrity assessments
If you fit the profile outlined above and you would like to discuss further, please send in your updated CV and call Nighat Rehman on .
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