Turnover Package Document Reviewer
- East Coast
- Contract
- Life Sciences
This vacancy has now expired
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
The candidate must have the rights to work in the location stated in the job advert.
Please note, Quanta part of QCS Staffing does not sponsor Visa applications.
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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 Quanta. 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
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.
Global Pharmaceutical firm
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