What are the responsibilities and job description for the Automation Downstream Process DeltaV Support Engineer position at QCS Staffing?
Automation Downstream Process DeltaV Support Engineer - North Carolina - 6 Months Contract
Our client, a global pharmaceutical manufacturing organization are looking for a talented Automation Downstream Process DeltaV 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:
Our client, a global pharmaceutical manufacturing organization are looking for a talented Automation Downstream Process DeltaV 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:
- Attend regularly scheduled project status meetings with Automation engineers and the System Integrator
- Attend weekly DSM Automation Huddle meeting to provide status to the DSM Automation Team
- Provide design review and input on Automation requirements for one or multiple process areas
- Attend and provide feedback during System Integrator functional reviews of certain process areas
- Review life cycle documentation
- Review and approve Kneat documents including: DeltaV software FATs, SATs, Automation Commissioning Test Protocols, software OQs, and Software Installation Verification protocols.
- Support generation of Kneat documents.
- Manage/oversee the System Integrator’s support of loop checks & commissioning activities for certain process areas
- Coordinate with various project workstreams including Automation, CSV, CQV, Utilities, Process Engineering, and others as needed
- Complete Safety, Project Procedure, and Project Instruction training as required
- Extensive direct experience working with Emerson DeltaV DCS
- Experience in a cGMP pharmaceutical facility working with FDA regulations is required
- Working knowledge of Kneat validation software is required
- Excellent organizational, oral, and written communication skills and fluency in English with the ability to effectively communicate within cross-functional teams and to management
- Excellent interpersonal skills and ability to work effectively and efficiently in a team-based environment with employees at all levels
- Ability to manage commitments while displaying an eagerness to learn and continuously improve
- Knowledge with Drug Substance Manufacturing (DSM) would be beneficial
- MasterControl, ComplianceWire, TrackWise, and Veeva experience is a plus
