R&D Partners is seeking an Engineering Validation Specialist to join a dynamic team in London.
In this role, you will ensure that all equipment, facilities, and computerized systems used in regulated processes meet the required standards. You will act as a subject matter expert on validation, ensuring compliance with EU, UK, and FDA regulations while supporting quality management activities.
Please note that to be considered for this role you must have the right to work in this location.
Responsibilities:
* Ensure all equipment, facilities, and systems are validated and compliant with regulatory requirements.
* Review and approve validation documents, protocols, and reports.
* Collaborate with various departments to align validation plans with business objectives.
* Support audits and inspections by acting as a subject matter expert.
* Address and resolve issues related to validation and compliance.
* Maintain inspection readiness and ensure documentation meets quality standards.
* Manage changes and deviations effectively, ensuring timely resolution.
* Stay updated on industry regulations and best practices.
Key Skills and Requirements:
* Experience working within a cGMP pharmaceutical/biotechnology manufacturing environment
* Knowledge of computerized system validation
* Experience working on equipment validation
For more information, please contact William Hay
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.
R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.
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