Validation Engineer - Pharmaceutical Processing & Manufacturing.
Our Client is a well-established expert in the pharmaceutical, nutraceutical, biopharmaceutical and biotechnology processing and manufacturing industries. They are now seeking a Validation Engineer . This position will be based near Southampton, Hampshire . The position is a full-time permanent role. Job Purpose To manage the design and production of all validation processes and qualification documentation packages for both in-house and external site related testing and qualification activities in accordance with the Companys Quality Management Procedures Key Responsibilities To be familiar with, and act in accordance with, all relevant health and safety management legislation To be familiar with, act in accordance with, and help develop the company quality systems rules, regulations and policies Works within corporate policies and frameworks, but also encouraged to influence directions taken on strategic issues To follow GAMP principles as appropriate, ensuring validation methods are consistent with the approach and that quality is built into each stage of the processes To provide comprehensive support in the issue, administration and control of all qualification related documents and the associated reference drawings and specifications To ensure all qualification documents including reference documents are completed, signed off and archived as appropriate before release of originals for execution to customers, both at FAT and the SAT (IQ / OQ) phase To conduct and assist the Project Team in the execution of Factory Acceptance Testing with or without customer attendance To liaise and consult with the in house commissioning team to ensure understanding of protocol execution procedure is understood To work in collaboration with all related departments to ensure delivery of protocols on time to project requirements To develop and communicate a clear option structure to allow Sales to offer appropriat...