CQV Engineer
- France
- Contract
- Commissioning, Qualification and Validation
This vacancy has now expired
Are you looking for your next contract, and fancy the opportunity to work in the beautiful Toulouse? Our client, a global biotechnology organisation, are recruiting for a CQV Engineer to join their team in the construction of their new biopharmaceutical production plant. This new build facility will be vital vehicle in helping our client continue global access to life changing therapeutics.
Role and responsibilities:
- Liaise with CQV PM and Lead Scheduler in relation to schedule creation and management for all Systems, ensuring all correct predecessors and successors are in place.
- 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 (Design/CM/CQV/Automation/Process/SMEs/Ops/Maintenance/PMs) to ensure all Systems are managed appropriately for the Project Lifecycle.
- Liaise with CQV Document Generation Lead in relation to generation and approval of; DQ/Design Reviews/SLIA/Test Matrices/Risk Assessments/QA Ven. or Assessments/FAT/SAT/CTP/IOQ Protocols
- Lead execution of all CQV deliverables; IOQ, field execution
- Run Weekly CQV Meeting and ensure updates are provided to Weekly CQV Meeting.
- Generate and ensure timely approval of all Commissioning and IOQ Final Reports.
Requirements:
- Minimum of 5 years’ experience including experince with expansion projects.
- Experience working with process equipment including; filtration systems, chromatography equipment and consumables, bioreactors, cell culture systems, mixing systems, bioprocessing containers, sterilisers, centrifuges, incubators, biosafety cabinets,.
- Experience with complex projects and working in or around operating facilities.
- Experience within process equipment within the pharmaceutical / biotech industries
- Ability to keep work pace and meet deadlines. Good organising and planning skills.
- Demonstrated proficiency communicating and collaborating at a variety of levels with customers, local vendors, equipment suppliers and operations staff.
- Proven success working well in a team environment with flexibility to react to changing business needs.
- Strong leadership and communication skills. Problem solver with a focus on achievement of overall project goals.
- Computer skills (Spreadsheets, Word Processing, Visio, Microsoft Project)
If this role is of interest to you, please apply now!
#LI-CO1
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
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