CQV PLC Support Engineer
- North America, United States
- Contract
- CAPEX Projects
Our client, a global pharmaceutical manufacturing organization are looking for a talented CQV PLC Support 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.
Essential Duties and Responsibilities for this role include, but are not limited to:
- CQV PLC Support Engineer for review and/or approval of all Automation CSV Master Plans, procedures, and other documents relevant to CQV scopes of work. This scope includes PAS, BMS, EMS, MES, Data Historian, OSI Pi and Equipment PLC systems.
- The Lead CSV CQV Engineer will be the single point of contact to the Automation CSV team and will participate in weekly meetings to ensure the CSV strategy and approach are aligned with CQV expectations and requirements.
- The Lead CSV CQV Engineer will be the eyes and ears for the CQV Team leads with respect to Automation Team deliverables thus ensuring seamless integration into the CQV strategy, schedule and test plans.
- Liaise with and support the CQV Buildings, Support Equipment and Clean Utility Teams, as well as interface with and support CQV Set to Work for GMP and non-GMP equipment and systems.
- Liase with Automation PM in relation to CSV portion of Project Schedule to identify and enable automation testing at appropriate times to facilitate the efficient startup of system and equipment. Coordinate and assist CSV Group for Project from Design through to PPQ Stage.
- Identify prerequisites as necessary for the testing of code to be used in support of CQV testing and inform the CQV scheduler to ensure prerequisite logic is included in the schedule.
- Aligning with Automation, reviewing Computer Systems Validation Master Project Plan for the Automation & IT computer Systems, PLAN- Validation Project Plan (VPP) for PAS and OEM Automation Computer Systems, PLAN- Validation Project Plan for OSI-Pi Site Historian and PLAN-Computerized Systems Validation Project PLAN for Standalone QC laboratory instruments.
#LI-MC1
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
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
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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