- Degree level or equivalent qualifications in applied biology or biochemical/biomedical engineering
- Good understanding of research & pharmaceutical manufacturing regulations.
- Experience in the Validation of Systems, equipment and environment.
- Experience of working in life science or healthcare environments
- Proven team working skills gained within in a project setting.
- Confident user of IT and in particular Microsoft Office Packages e.g., Word, VISIO, Projects, Excel, Outlook
- Highly organised and methodical with attention to detail
- Willingness to travel
- Experience of working in a Clean Room or Laboratory environment
- Knowledge in any of the following areas, GLP, GMP, biomedical, biocontainment, pharmaceutical manufacturing, or fumigation processes
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GMP Validation Officer - Peterborough, United Kingdom - CY Partners
Description
CY Partners are currently looking to recruit two GMP Validation Officers on behalf of a UK based organisation that offers the validation, design, development and safe operation of Laboratories and Aseptic Facilities for leading Life Sciences and Healthcare institutions.
This is a Customer Facing role which will require regular travel to sites across the UK.You must ensure required quality and safety standards are achieved and maintained with respect to cGMP procedures, all cGMP validation documentation is tracked, ensuring compliance with regulatory and legislative requirements.
You will assist the management of the GMP projects from new business interest, feasibility through to construction and completion. Generating the full life cycle of validation documentation to support customer projects. Participating and facilitating regular customer meetings.Requirements
