Validation Engineer

Do you have validation engineering experience working in a GMP Life Science or Healthcare environment? Do you have expertise in clean rooms and biocontainment? Are you looking for an exciting and unique challenge with a rapidly growing business?

Our client are a specialist life science and healthcare company who work with a range of clients including universities, pharmaceutical manufacturers and the NHS. They provide expert consultancy in clean room environments, biocontainment and laboratory set-up, supporting clients to establish new laboratories and expand existing facilities.

Due to growth, they are looking for an experienced Validation Engineer with proven GMP life science or healthcare experience, including practical expertise in cleanroom validation. This is an exciting opportunity to join a rapidly growing business and support complex projects for clients across healthcare, pharmaceutical manufacturing, and research environments.

Responsibilities will include Lead Projects through all stages of design and development Working with a project team of end users, designers and contractors to deliver high quality projects to timescale Provide detailed consultancy to project stakeholders in line with regulatory and engineering standards for clean room design and construction Execution of validation protocols at customer and vendor facilities Generation of Quality Risk assessments Lead project meetings including site visits Generation of Validation Protocols for a full validation life cycle. Producing documentation specific to customer

requirements

URS, VMP VP, RTM, DQ, IQ, OQ, & VSR. Responsible for the review, creation and maintenance of project progress reports including internal reports on project progress against budget and costs Implement continuous improvement suggestions on process, procedures and documentation To be considered for the role you will have Scientific graduate and post-graduate qualifications in applied biology, biochemical/biomedical engineering Understanding of SHE, ensuring compliance with regulatory and legislative requirements.

A strong understanding of GMP requirements within research & pharmaceutical manufacturing regulations or healthcare environments Familiar with Cross contamination control strategies & Quality Risk assessments. Experience in the Validation of systems, equipment, and environment.

Demonstrable experience validating systems, utilities, equipment, controlled environments, and associated facilities. Experience of project delivery Highly organised and methodical with attention to detail Able to maintain confidentiality of Company and clients' information. Hands on experience of working i...

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