DeltaV Engineer - 5+yrs Experience - Dublin, Cork, Tipperary

Posted 15 Days Ago
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Cork, IRL
In-Office
Senior level
Automotive
The Role
Design, develop, configure and support DeltaV control systems (including Batch) for biopharma projects. Produce design and lifecycle documentation (GAMP), modify control modules and phases, attend team meetings, lead project tasks, and ensure regulatory compliance and validation in a regulated environment.
Summary Generated by Built In

PACIV, a global leader in industrial automation solutions with offices in Puerto Rico, United States and Ireland, and servicing the Life Sciences, F&B and Utilities industries, is looking for Delta V Engineer with 5+ years experience.for our clients in Cork, Tipperary and Dublin

Job Description:

The potential candidates must have 5+Years Delta V Experience, including Batch.

Position Responsibilities /Essential Functions

  • Be part of a project team contributing to the completion of a biopharma project based on the Delta V platform.
  • Support the project on a day-to-day basis for Delta V System including:
  • Design document generation.
  • Code development and modification.
  • Batch configuration.
  • Lifecycle documentation generation in line with GAMP (FS, DS, SDS and associated test documents).
  • Modifications to control modules.
  • Generation of new and existing equipment modules.
  • Modification to phase modules.
  • New phase modules generation.
  • Attending daily team meetings.
  • Project leadership.
  • Familiarity with biopharma processes.

Requirements:

  • Education: Bachelor’s degree in Engineering (preferably Electrical, Automation, Instrumentation or Chemical).
  • Work Experience: From 3+ years of industrial automation experience.
  • Experience in the life sciences industries is preferred.
Desired Hard Skill Sets:
  • Design, programming, implementation and support for control system/automation projects within regulated environment.
  • Comprehensive understanding of, Delta V including Batch essential. Knowledge of other control systems e.g Siemens, Allen Bradley, programmable logic controllers (e.g. Micrologix, Logix 5000) and HMI/SCADA systems (e.g. iFix, RSView, Wonderware, Batch) desired.
  • Knowledge of Alarm Management, Data Historian, OEE desired.
  • Knowledge and experience of computer system life cycle concepts and FDA regulatory requirements, including 21 CFR Part 1 desired.
Desired Soft Skills:
  • Excellent analytical and problem-solving skills to be applied in electrical design, programming and troubleshooting of process and packaging systems.
  • Deals well with uncertainty and pressure.
  • Works well with others, within a team and takes accountability.
  • Result driven and self-motivated.
  • Fluent in English.
  • Strong interpersonal and communication skills (verbal and presentation).
  • Organized, with strong computer literacy such as Excel, etc.


Other Requirements
Location: Multiple sites, Cork, Dublin, Tipperary

Travel: To clients, suppliers within Ireland

Compensation:

Regular staff position, competitive salary and employee benefits package .

Job Type: Permanent, or contract

PLEASE NO AGENCIES

Skills Required

  • Bachelor's degree in Engineering (Electrical, Automation, Instrumentation or Chemical)
  • 5+ years DeltaV experience including Batch
  • 3+ years industrial automation experience
  • Experience in the life sciences industries
  • Design, programming, implementation and support for control system/automation projects within a regulated environment
  • Comprehensive understanding of DeltaV including Batch
  • Knowledge of Siemens and Allen Bradley PLCs (MicroLogix, Logix 5000)
  • Knowledge of HMI/SCADA systems (iFIX, RSView, Wonderware)
  • Knowledge of Alarm Management, Data Historian, OEE
  • Knowledge of computer system life cycle concepts and FDA regulatory requirements (e.g., 21 CFR) and GAMP documentation
  • Fluent in English
  • Strong analytical, problem-solving, interpersonal and communication skills; organized with computer literacy (e.g., Excel)
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The Company
HQ: 65th Infantry, PR
103 Employees
Year Founded: 1997

What We Do

PACIV, Inc. (Process Automation – Controls.Instruments.Validations) was founded and registered as a corporation in the Commonwealth of Puerto Rico in 1997. Listening to our clients'​ desire for local support and standardization among their facilities, we opened our Indiana office (PACIV-USA, LLC) in 2003. Moreover, in 2011 we opened PACIV-Ireland in Cork, Ireland. Our expansion, including international presence with local resources, responds to the needs of our Life Sciences multinational clients regarding replication and consistency of implementation, who demand our life sciences automation and regulatory compliance solutions in a localized market format. Our thorough understanding of the challenges faced by the Life Science sector and our collaborative approach with our clients has enabled us to become a leading Life Sciences automation and regulatory compliance service company. Since our inception, we provide our Life Sciences clients with our services in their multiple manufacturing sites worldwide. The fact that we hold Master Service Agreements (MSA’s) and Preferred Vendor status with the world’s leading Life Science Companies serves a testimony of our quality of service and leadership standing within the Life Science industry. We attract and develop the best talent which allows us to provide our demanding clients with the right knowledge and expertise ensuring we provide significant value within our automation solutions and services.

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