What are the responsibilities and job description for the Automation Engineer - Deltav position at ExecutivePlacements.com?
Day To Day
Our client in Raleigh-Durham is seeing a Process Automation DeltaV Support Engineer to join their team. This individual will support the system integration management for both downstream and upstream equipment. Equipment is controlled primarily by a DeltaV DCS and Syncade is the MES. The System integrator will update DeltaV configuration from code received from the corporate headquarters to align with site-specific equipment requirements. This role will require coordination with and management of the System Integrator.
The following scope will be provided by the Process Automation DeltaV Support Engineer:
Attend regularly scheduled project status meetings with Automation engineers and the System Integrator
Attend weekly 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 Integrators 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
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal. com. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
Pluses
Experience supporting upstream or downstream equipment
Knowledge with Drug Substance Manufacturing (DSM) would be beneficial
MasterControl, ComplianceWire, TrackWise, and Veeva experience is a plus
Must Haves
4 years direct experience working with Emerson DeltaV DCS experience with configuration, updating batches, phases and recipes.
Experience in a cGMP pharmaceutical facility working with FDA regulations is required
Working knowledge of Kneat validation software
Excellent organizational, oral, and written communication skills and fluency in English with the ability to effectively communicate within cross-functional teams and to management
Our client in Raleigh-Durham is seeing a Process Automation DeltaV Support Engineer to join their team. This individual will support the system integration management for both downstream and upstream equipment. Equipment is controlled primarily by a DeltaV DCS and Syncade is the MES. The System integrator will update DeltaV configuration from code received from the corporate headquarters to align with site-specific equipment requirements. This role will require coordination with and management of the System Integrator.
The following scope will be provided by the Process Automation DeltaV Support Engineer:
Attend regularly scheduled project status meetings with Automation engineers and the System Integrator
Attend weekly 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 Integrators 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
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal. com. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
Pluses
Experience supporting upstream or downstream equipment
Knowledge with Drug Substance Manufacturing (DSM) would be beneficial
MasterControl, ComplianceWire, TrackWise, and Veeva experience is a plus
Must Haves
4 years direct experience working with Emerson DeltaV DCS experience with configuration, updating batches, phases and recipes.
Experience in a cGMP pharmaceutical facility working with FDA regulations is required
Working knowledge of Kneat validation software
Excellent organizational, oral, and written communication skills and fluency in English with the ability to effectively communicate within cross-functional teams and to management