Process Validation Manager
An exciting opportunity has become available at a leading biopharmaceutical / medical devices organisation. The roe is a for Process Validation / Technical Development and QC Manager who will oversee changes within Biological Manufacturing to drive improvements in both compliance and efficiency using structured processes.
In this role, you will provide leadership to your team who are responsible for ensuring that critical processes & equipment used within manufacturing are used effectively and are fully validated.
•Validating new processes, materials or equipment developed either during New Product Development (NPD) or Change Control.
•Evaluate and improve existing processes, materials or equipment used within manufacturing. This may include the identification & the selection of new equipment via the use of process methodologies, risk assessments, FMEA etc.
•Contribute to the process of defining the performance and specification of new products.
•Critically assess raw materials and generate raw material specifications including QC limits for all new components parts.
•Carry out new product feasibility studies, designing working reagents as defined in the New Product Development process.
•Knowledge of chromatography techniques at multiple scales.
This is an excellent opportunity with a growing company. The site has excellent public transport links and plenty of free parking, as well as a very competitive benefits package.
The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. CY Partners Recruitment Ltd, trading as CY Partners is an Employment Business/Agency.
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