Upstream Process Automation DeltaV Support Engineer

Position Title & Basic Details

Were looking for an Upstream Process Automation DeltaV Support Engineer based in NC. This is a Contract position requiring 5+ years of relevant experience. A Bachelors degree in Engineering or a related field is strongly preferred.

Overview

In this role, you'll be responsible for supporting system integration management for upstream equipment and systems within the Drug Substance Manufacturing (DSM) area. The ideal candidate brings a solid foundation in Emerson DeltaV DCS and thrives in a collaborative environment.

Key Responsibilities

• Attend regularly scheduled project status meetings with FDBN Automation engineers and the System Integrator
• Attend weekly DSM Automation Huddle meetings to provide status updates 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 and oversee the System Integrators support of loop checks and 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

Requirements

• Education: Bachelors degree in Engineering or a related field or equivalent experience.
• Technical Expertise: Proficiency in Emerson DeltaV DCS; familiarity with Kneat validation software required.
• Experience: Minimum 5 years working with DeltaV DCS in a cGMP pharmaceutical facility, experience with FDA regulations.
• Soft Skills: Excellent organizational, oral, and written communication skills; excellent interpersonal skills; ability to manage commitments while displaying eagerness to learn and continuously improve.

Preferred Qualifications

• Knowledge of Drug Substance Manufacturing (DSM)
• Experience with Master Control, Compliance Wire, Track Wise, and Veeva

Why Join Us?

• Growth Opportunities: Work with a team that will enhance your technical development.
• Innovative Environment: Engage with cutting edge technologies and challenging projects.
• Team Culture: Join a collaborative group that values teamwork, transparency, and innovation.

Interview Process

• Virtual Interviews: Conducted via Teams/Zoom/etc.

Additional Information

• Must be authorized to work in the U.S. (US Citizen, Green Card, or valid Work Permit)
• Ability to attend in person interviews as necessary
• Job type: Contract position
• Fulltime
• Onsite role
• Duration: 6-12 Months
• Ref#: L9WV5744