Validation Engineer
Location: 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 is a specialist life science and healthcare company working 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, delivering a high level of service to support clients in establishing new laboratories and expanding existing ones. Due to growth, they are now recruiting a Validation Engineer to join their team.
Responsibilities
- Lead projects through all stages of design and development
- Work 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
- Execute validation protocols at customer and vendor facilities
- Generate Quality Risk assessments
- Lead project meetings including site visits
- Generate validation protocols for a full validation life cycle
- Produce documentation specific to customer requirements: URS, VMP, VP, RTM, DQ, IQ, OQ and VSR
- Review, create and maintain project progress reports, including internal reports on project progress against budget and costs
- Implement continuous improvement suggestions on process, procedures and documentation
Qualifications
- 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 and pharmaceutical manufacturing regulations – GMP
- Membership of a relevant professional body
- Familiar with cross‑contamination control strategies and quality risk assessments
- Experience in the validation of systems, equipment and environment
- Experience of project delivery
- Highly organised and methodical with attention to detail
- Ability to maintain confidentiality of company and clients’ information
- Experience 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 and 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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