My client is working to enable ATMP manufacturers bring autologous medicines to more patients. Using their smart technology, they are driven to make this highly specialised area of medicine deliverable, available and most of all, affordable.
Their bespoke software cuts huge amounts of administrative resource that supports the manufacturing process. As a result, more treatments will be available to happen simultaneously while enhancing quality assurance and security of the supply chain and data.
They are now looking to bring in a CSV Specialist to assist in defining the validation strategy and approach taking into account the relevant GxP requirements as the primary subject matter expert (SME) for CSV.
> You#39&ll need to have a Bachelor’s degree in a Scientific or Technical discipline
> 5+ years’ experience working within validation and complex computer systems
> Proven industry experience in a CSV role within the pharmaceutical industry.
It#39&s an exciting time to join a fast growing, innovative start-up who are striving to impact the lives of thousands of cancer patients.
Get in touch ASAP to learn more about this exciting company, and how you could become an integral member of the team!
******please note this client is actively recruiting*****
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