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Clean Room Validation Specialist
2 months ago
Job Summary
CY Partners is seeking a highly skilled Clean Room Validation Specialist to join our team on behalf of a leading UK-based organization that specializes in the validation, design, development, and safe operation of laboratories and aseptic facilities for top-tier life sciences and healthcare institutions.
This is a customer-facing role that requires regular travel to sites across the UK. As a Clean Room Validation Specialist, you will be responsible for ensuring that quality and safety standards are achieved and maintained in accordance with cGMP procedures. You will also be responsible for tracking and ensuring compliance with regulatory and legislative requirements.
Key Responsibilities
- Assist in the management of GMP projects from new business interest to feasibility, construction, and completion.
- Generate full life-cycle validation documentation to support customer projects.
- Participate in regular customer meetings and provide expert validation guidance.
- Collaborate with cross-functional teams to ensure seamless project execution.
- Develop and maintain strong relationships with customers and stakeholders.
Requirements
- Degree-level or equivalent qualifications in applied biology or biochemical/biomedical engineering.
- Excellent understanding of research and pharmaceutical manufacturing regulations.
- Proven team working skills gained within a project setting.
- Confident user of IT and Microsoft Office Packages (e.g., Word, VISIO, Projects, Excel, Outlook).
- Willingness to travel and work in a fast-paced environment.
- Experience working in a clean room or laboratory environment.