Engineering Validation Specialist

R&D Partners is seeking an Engineering Validation Specialist to join our team in The UK. In this role, you will provide essential support for validation processes related to equipment, facilities, and computerized systems. You will ensure compliance with regulatory standards and internal policies while collaborating with various departments to maintain operational excellence.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Support and oversee validation activities to meet EU, UK, and FDA regulatory requirements.
• Review and approve validation protocols, reports, and documentation.
• Collaborate with teams across departments to align validation plans with business goals.
• Act as a subject matter expert during inspections and audits, providing necessary documentation and responses.
• Ensure all equipment and facilities are qualified and maintained throughout their lifecycle.
• Address and resolve issues related to compliance, change controls, and deviations.
• Maintain inspection readiness and ensure all tasks comply with Good Manufacturing Practices (GMP) and internal quality systems.

Key Skills and Requirements:

• Experience within pharmaceutical/biotechnology manufacturing
• Experience carrying out equipment validation and CSV
• Right to work within the UK

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.

By submitting this application, you confirm that you’ve read and understood our privacy policy, which informs you how we process and safeguard your data – https://www.r-dpartners.com/privacy-policy/