CQV Clean Utilities Engineer
- North America, United States
- Contract
- CAPEX Projects
Our client, a global pharmaceutical manufacturing organization are looking for a talented CQV Clean Utilities 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.
Essential Duties and Responsibilities for this role include, but are not limited to:
- CQV Support Engineer for Clean Utilities, initially responsible for issue and review of all FAT wraparounds, DQ, RTM and QRA activities, then IOC/SAT and IOQ, including SR’s. Also review of all Design deliverables including Drawings, Datasheets, specifications and Engineering Lists.
- Aligning with System boundaries and Support and review exercise.
- Point CQV person for Vendor review for all Clean Utility Vendor Packages.
- CQV SME for all Clean Utility Systems.
- Liaise construction readiness and a schedule for all Clean Utility systems, perform and Support all field walk downs for all Clean Utility systems.
- Support CQV review, aligning with Transition Group in relation to review and approval of all Turnover Packages, both Vendor and Contractor Packages.
- Support CQV SWAT Team in relation to punchlist closure both pre-M/C and during the CQV execution phase.
- Liaise with CQV PM and Support Scheduler in relation to schedule creation and management for all Clean Utility Systems, ensuring all correct predecessors and successors are in place.
- Ensure Commissioning readiness of all Clean Utility Systems to support Equipment Start-up and IOQ Testing.
- Support PSSR/STW field execution and guide CQV Team through Start-up exercise in a safe and controlled manner.
- Extensive CQV Clean Utility experience on Large Scale Projects
- SME on both Clean and Black Clean Utility Systems
- Working knowledge of ASTM E2500 / Leveraging Verification process
- Extensive Clean Utility experience including experience with design and construction projects for biopharmaceutical manufacturing facilities.
- Experience with complex projects and working in or around operating facilities.
- Ability to keep work pace and meet deadlines. Good organizing and planning skills.
- Demonstrated proficiency communicating and collaborating at a variety of levels with customers, 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)
#LI-NR1
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
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
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