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Register interestAre you driven to uphold the highest standards in pharmaceutical quality control? Step into this role where your expertise ensures operational integrity and supports the delivery of safe, effective treatments worldwide.
R&D Partners is seeking a QC Validation Specialist to support the development, validation, and transfer of analytical test methods for gene therapy products. This role ensures compliance with EU and FDA GMP standards while maintaining data integrity and quality control processes. You will play a key role in ensuring methods are validated, transferred, and implemented effectively within GMP labs.
Please note that to be considered for this role you must have the right to work in this location.
Responsibilities:
Key Skills and Requirements:
For more information, please contact Jessica Taylor.
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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If you can’t find your ideal role with us right now, we’d still love to hear from you! Send us your CV and we’ll contact you if a suitable role becomes available.
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