Duration: 12-Month Contract
Our client, a global pharmaceutical manufacturing organization are looking for a talented IV CQV Engineer to join their expanding team. With continued organizational growth and considerable investment across their portfolio and capital programs this is an extremely exciting opportunity to contribute towards their brand-new manufacturing facility on the East Coast of the United States.
Key Responsibilities:
Review of turnover packages from vendors and construction
Walk systems to ensure installation is right (knows how to walk and read P&IDs)
Can work alone once direction is given on what to do
Ensure that IV execution is done according to engineering specifications, CQV procedures, CQV project strategies, and industry standards such as BPE commissioning and validation guidelines.
Liaise with Jacobs and FDBN concerning the quality of documentation construction for utilization of qualification.
Coordination with CQV handover for checking and validation purposes on all Packages Turn-over-Over VTOPs, as well as on CTOPs.
Coordination with the SWAT team for handover punchlists. These can both be carried out either pre-MC and also throughout the course of CQV execution.
Liaise with all Project Groups (Design/CM/CQV/Automation/Process/SMEs/Ops/Maintenance/PMs) to ensure all Systems requiring IV execution are managed appropriately.
Liaise with System Owners (Responsible Engineers) for IV tasks, including but not limited to specification deviation requests, PCC impact to test cases, and vendor documentation gaps.
Coordinate timelines and needs for required IV pre-req documents, including but not limited to VDRs for IV execution, VDRs for OV execution start, QAM reports, CTOP test pack deliverables, and passivation and pressure test documentation from vendors, CMT, and STW activities.
Apply now: https://www.qcsstaffing.com/Apply?jid=7109