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Lead CQV Turnover & QA Engineer

  1. East Coast
  1. Contract
Competitive
  1. Life Sciences
26-05-2023
31456

This vacancy has now expired

Lead CQV Turnover & QA Engineer- Life Science- Contract – North Carolina

Our client, a global Pharmaceutical manufacturing organization are looking for a talented Lead CQV Turnover & QA 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.

Lead CQV Turnover & QA Engineer Responsibilities:
  • Lead Turnover/QA Engineer for whole Project will ensure we have a seamless turnover from the Design phase into Construction and through the CQV Phase.
  • Lead and be responsible for CQV review of all Equipment Packages, Vendor Data Requirements (VDR) and detailed Table of Contents (TOC) for both Vendor Packages and Construction stick-built packages.
  • Liaise with Engineering Firm to ensure all quality objectives are being met in relation to pre-construction readiness (review of Quality Plan, Construction Check sheets).
  • Lead Blended Project Team in relation to Receipt Verification (RV), in both Plan development, setting up for RV and RV execution.
  • Align with QA and Lead Vendor Assessments for all Direct Impact Vendors, performing detailed assessment at vendor’s premises, ensure all quality objectives are met and any items found are tracked to closure.
  • Pre Mechanical Completion, responsible for the reviewing of all VTOP and CTOP, in readiness of IQ checks.
  • Lead CQV review on all Isometrics, Weld logs, Weld Qualifications, 3rd Party Inspections, Material of
  • Construction, Redlining exercise and walk down coordination.
  • Coordinate punch-list close-out for all systems, aligning with the Engineering firm pre-M/C and CQV Teams post M/C and up until PQ complete.
  • Support CQV Work streams in relation to field execution and document review and approval

About you:
  • Minimum of 10years of Turnover experience including experience with design and construction projects for biopharmaceutical manufacturing facilities.
  • Minimum 5years experience in Leading Turnover/Blue Tag Teams
  • 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 (Primavera, Spreadsheets, Word Processing, Visio, Microsoft Project)
 


Are you a good fit for a Lead CQV Turnover & QA Engineer? Get in touch with us today.

 




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