CQV Downstream Engineer
- All US
- Contract
- CAPEX Projects
This vacancy has now expired
Our client, a global Pharmaceutical manufacturing organization are looking for a talented CQV Downstream 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.
Main Responsibilities:
- CQV Engineer for Equipment in the Downstream Area for the DSM Building, initially responsible for review of all Design deliverables from Jacobs Engineering including Drawings, Datasheets, specifications and Engineering Lists.
- Support generation of all CQV DST Documentation – FAT wraparounds, DQ, RTM, QRA, SAT/IOC and IOQ, including Final Reports.
- Generate DST Bridging document, ensuring full alignment with Process Science (PS) in relation to supply of CPPs and CQAs.
- Point CQV person for Vendor review for all DST Vendor Packages. CQV SME for all DST Systems.
- Liaise with Engineering in relation to construction readiness and a schedule for all DST systems, perform and lead all field walkdowns for all systems.
- Lead CQV review, aligning with Transition Group in relation to review and approval of all Turnover Packages, both Vendor and Contractor Packages within the Process Equipment Support scope.
- Liaise with CQV SWAT Team in relation to punchlist closure both pre-M/C and during the CQV execution phase for all Process Equipment Support systems.
- Liaise with CQV PM and Lead Scheduler in relation to schedule creation and management for all DST Systems, ensuring all correct predecessors and successors are in place.
- Ensure Commissioning readiness of all DST Systems to support Equipment Start-up and IOQ Testing.
Requirements:
- Minimum 3 years CQV DST Equipment experience on Large Scale Projects
- SME on all DST Systems, minimum 3 years
- Working knowledge of ASTM E2500 / Leveraging Verification process
- Experience with liaising with other departments and building PMs/leads
- Minimum of 3 years of Equipment experience including experience with design and construction projects for biopharmaceutical manufacturing facilities
- Minimum 3 years experience in Leading Equipment CQV Team
- Experience with complex projects and working in or around operating facilities
- 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
If this role is of interest to you, please apply now!
I have always received a highly professional & personable service from the team at QCS Staffing. 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
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing'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 QCS Staffing'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
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