Validation Engineer
Surrey
Salary/Rate: £45,000-55,000
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 advice and knowledge in relation to clean room environments, biocontainment and laboratory set-up, providing a high level of service in order to support their clients achieve their goals with relation to establishing new laboratories and expanding existing ones. Due to growth, they are now looking to recruit a Validation Engineer to join their team.
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
- Scientific graduate and post-graduate qualifications in applied biology, biochemical/biomedical engineering
- Understanding of SHE, ensuring compliance with regulatory and legislative requirements.
- Good understanding of research & pharmaceutical manufacturing regulations – GMP.
- Membership of relevant professional body
- Familiar with Cross contamination control strategies & Quality Risk assessments.
- Experience in the validation of systems, equipment, and environment.
- Experience of project delivery
- Highly organised and methodical with attention to detail
- Able to maintain confidentiality of Company and clients’ information.
- Experience of working in a Clean Room or Laboratory environment
- Knowledge of, GLP, GMP, biomedical, biocontainment, pharmaceutical manufacturing, or fumigation processes
- Understanding of cGMP Clean Rooms, cGMP related utilities maintenance, cGMP equipment engineering & maintenance, Validation, and warehousing for cGMP related materials /product storage.
- Familiarity with the RIBA stages of design.
- Willingness to travel on a regular basis
You will be rewarded with a friendly, inclusive working environment and competitive salary, as well as the opportunity to join a great business at an exciting time.
For more information or to apply, please contact Chris Vinter.
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