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CQV Engineer- UK, Yorkshire - 9 Month Contract
Our client, a global CDMO in pharmaceutical manufacturing, is recruiting for a CQV Engineer to join their new and exciting large-scale CAPEX investment programme. With a mission to provide process development and cGMP production in cell culture, microbial fermentation, and gene therapies, this is an outstanding opportunity make a genuine contribution to the biopharmaceutical industry.
Responsibilities Include
* Liaise with CQV PM and Lead Scheduler.
* Ensure Commissioning readiness of all Systems to support Equipment Start-up and IOQ Testing.
* Lead CQV interface with EIDA / or Master Project Database equivalent system, ensure full traceability at all times for all systems within the fill finish building
* Liaise with all Project Groups to ensure all Systems are managed appropriately for the Project Lifecycle.
* Lead execution of all CQV deliverables; IOQ, field execution
* Responsible for the generation of Test Protocols for the verification of process equipment.
* Execution of the protocols utilising data generated by equipment vendors.
* Execution of any remaining testing requirements.
* Oversight of vendor testing.
* Generation of reports.
Key requirements include:
* Extensive experience including experience with expansion projects.
* Experience working with process equipment including; filtration systems, chromatography equipment and consumables, bioreactors, cell culture systems, mixing systems, bioprocessing
If this role is of interest, please apply now!
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Contract
Job function
* Job function
Engineering and Information Technology
* Industries
Staffing and Recruiting
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