| CQV CIP Engineer at Remote, Remote, USA |
| Email: [email protected] |
|
From: shrasti singh, vyzeinc [email protected] Reply to: [email protected] Job Description - CQV CIP Engineer North Carolina (Onsite) USC/GC 12 MONNTH Job description Responsibilities CQV Support Engineer for all CIP Equipment in the DSM Buildings, initially responsible for review of all Design deliverables from Jacobs including Drawings, Datasheets, specifications and Engineering Lists. Support generation of all CQV CIP Documentation FAT wraparounds, DQ, RTM, QRA, SAT/IOC and IOQ, including Final Reports. Point CQV person for Vendor review for all CIP Vendor Packages. CQV SME for all CIP Systems. Produce CIP Bridging to include all CCP, CQAs and worst case information of circuits. Support all circuit reviews for all CIP routes and circuits, working out worst case scenarios for testing and cleaning requirements. Liaise with construction manager in relation to construction readiness and a schedule for all CIP systems, perform and Support all field walkdowns for all systems. Support 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 Support Scheduler in relation to schedule creation and management for all CIP Systems, ensuring all correct predecessors and successors are in place. Ensure Commissioning readiness of all CIP Systems to support Equipment Start-up and IOQ Testing. Requirements Extensive Equipment experience on Large Scale Biopharmaceutical Projects SME on all CIP Systems, minimum 5 years Working knowledge of ASTM E2500 / Leveraging Verification process Experience with liaising with other departments and building PMs/leads Minimum of 10 years of Equipment experience including experience with design and construction projects for biopharmaceutical manufacturing facilities. Minimum 5 years' experience on Equipment CQV Team 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) Keywords: cprogramm green card CQV CIP Engineer [email protected] |
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| 03:27 AM 04-Mar-25 |