Turnover Package Document Reviewer- Life Science- Contract- North Carolina

Our client, a global Pharmaceutical manufacturing organization are looking for a talented Turnover Package Document Reviewer 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.

Turnover Package Document Reviewer Responsibilities:

Responsible for the initial set-up of the Project Document Control System, utilizing Scope, EIDA, JPI, and DCA, as the electronic document management systems, for Non-qualified and Qualified systems.
Aligning with CQV leads, created templates for all stages of the project testing
Set-up initial audit forms for all direct impacting vendors, to ensure at contract award stage that all QMS (Quality Management System) audits had been completed, passed and documented
Created Table of Contents and Templates for all TTOPs (Trade Turnover Packages) and VDR’s for VTOPs (Vendor Turnover Packages)
Utilise system to support P&ID walk-downs
Daily control and issue of all Project Documents (Drawings, Specifications, SOP’s Procedures, Protocols)
Carried out DCC and GDP Training for all Project personal
Post execution – scanning of all GMP Documentation – DCA
Control of all as-built documentation (P&IDS, SLD, Loop Diagrams) to support the BT process
Utilise EIDA Master Project Database to update redlined information for VTOP’s.
Coordination of all Project Punch list information, through Project Lifecycle, ensuring timely closure of all punch items at different Stage Gates.
Liaise with Construction at M/C Stage to ensure all documentation is correct at time of system walk-downs and also and full MC sign-off
Support Engineering Turnover Team in relation to the review and approval of all Piping Test
Packs and Electrical and Instrumentation Handover Packs
Control and issue of all CQV Set to Work (STW) documents, ensuring pre-approval for startup and post approval when all operational execution is completed, there-after, scanning of STW's into scope

Are you a good fit for a Turnover Package Document Reviewer? Get in touch with us today.

The candidate must have the rights to work in the location stated in the job advert.

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We have worked together with Quanta for seven years now and have always received a professional service. Quanta’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 Quanta’s people and their ability to deliver.

Engineering Director
Global Pharmaceutical firm

List #1

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