CQV Process Support Equipment
- North America, United States
- Contract
- CAPEX Projects
Our client, a global pharmaceutical manufacturing organization are looking for a talented CQV Process Support Equipment 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 for all Process Support and Miscellaneous Equipment Systems. Work with CQV PSE Team from initial design to final Handover.
- Liaise with Jacobs in relation to construction readiness and a schedule for all Process Support and Miscellaneous Equipment systems,
- Involved in field walkdowns for all systems.
- Involved in CQV review, aligning with Transition Group in relation to review and approval of all Vendor and Contractor Turnover Packages within the Process Support and Miscellaneous Equipment scope.
- Liaise with CQV SWAT Team in relation to punch list closure both pre-M/C and during the CQV execution phase for all Process Support and Miscellaneous Equipment systems.
- Liaise with CQV PM and Lead Scheduler in relation to schedule creation and management for all Process Equipment Support, ensuring all correct predecessors and successors are in place.
- Ensure Commissioning readiness of all Process Support and Miscellaneous Equipment Systems to support Equipment Start-up and IOQ Testing.
- Involved in PSSR/STW field execution and work with CQV Team through Start-up exercise in a safe and controlled manner.
- Work with CQV Process Support and Miscellaneous Equipment with EIDA and ensure full traceability at all times for all systems.
- Extensive CQV Equipment experience on Large Scale Projects
- Experience with Process Equipment Support Systems,
- Working knowledge of ASTM E2500 / Leveraging Verification process
- Extensive Equipment 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.
- Computer skills (Spreadsheets, Word Processing, Visio, Microsoft Project)
#LI-MC1
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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