Automation Controls Engineer (ONSITE) Job at PACIV-USA, LLC

PACIV-USA, LLC Indianapolis, IN 46218

PACIV, an international control systems integration and regulatory compliance engineering firm, servicing Bio-Pharmaceutical, Medical Device, Food and Beverage and Utilities clients, is looking for regular employment-based Automation Engineer at our USA office (Indianapolis office).

Job Description:

The Automation Engineer will be responsible for the implementation of industrial automation solutions, specifically in the utility and life sciences industries. Projects may include small scope changes to unit processes to large site-wide controls solutions. The automation engineer will be responsible for multiple projects and deliverables and will serve as the primary client interface for assigned projects.

Position Responsibilities/Essential Functions

  • Project Management – Track project scope, budget, and schedule. Responsible for thorough understanding of project scope and definition of hardware, documentation, and software deliverables. Serve as primary client liaison on assigned projects.
  • Conceptual Control System Design – Define and Interpret client control system requirements to recommend and design a complete computerized control system. This includes definition of process control, plant control networks, computers and virtualization, and software.
  • Electrical Control Panel Design – Select components and author drawing sets in AutoCAD Electrical for PLC-based systems, VFD and motor controls by following industry standards.
  • Instrumentation – Select and propose process instrumentation (flow, level, pressure, etc.).
  • Software Design and Implementation – Develop project programming standards, develop PLC code, develop graphical user interfaces. Install software platforms and developed application code on production systems.
  • Assembly and Fabrication – Aid in the assembly of designed control panels and systems. Support field installation and modifications of existing PLC systems and control circuits.
  • Troubleshooting – Provide technical support, problem solving, maintenance, modifications, and continuous improvement for automated equipment and process control systems.
  • Documentation – Prepare project submittals with may include requirements, design, test protocols, and operation and maintenance instructions.
  • Validation – Develop and/or support the generation and execution of validation lifecycle documentation in the life science industry.

Requirements

  • Education: Bachelor’s degree in Engineering, Engineering Technology, or equivalent experience. Preferred degrees: Chemical Engineering, Electrical Engineering, Mechatronics, Electrical Engineering Technology or similar.
  • Minimum of five (5) years automation experience.

Desired Hard Skill Sets:

  • Familiarity with processes within the pharmaceutical, biotechnology, and utility industries
  • Experience in authoring PLC, HMI, and SCADA applications.
  • Experience in troubleshooting DCS, PLC, HMI, SCADA, VFD, and electrical control circuits.
  • Experience with Allen Bradley (RSLogix5/500/5000, Studio5000), iFix, WonderWare, DeltaV, Siemens S7, Omron.
  • Experience with industrial communication networks (Ethernet, DeviceNet, ControlNet, Modbus, BACNet, DH+, Profibus, ProfiNet)
  • Comprehensive understanding process control systems related documentation (e.g., P&ID’s, URS, FS, DS).
  • Knowledge of Data Historian (OSIPI)
  • Knowledge of the Software Development Lifecycle (SDLC), Computer System Validation lifecycle and FDA regulatory requirements.
  • Experience and knowledge of PID Loops and loop tuning practices.
  • Experience implementing VFD controlled applications.
  • Proficient with AutoCAD, Electrical package preferred.
  • Understanding of electrical standards (NFPA 70E, UL508A, UL698, EIC, JIC, CE, ATEC)
  • Knowledge of S88 Standard; Configuration experience with FactoryTalk Batch and/or DeltaV Batch desired.

Desired Soft Skills:

  • Strong work ethic and customer service mentality.
  • Excellent analytical and problem-solving skills
  • Familiarity with processes within the pharmaceutical, biotechnology, and utility industries
  • Comfortable with 24/7 manufacturing environment
  • Deals well with uncertainty and pressure.
  • Works well with others, within a team and takes accountability.
  • Result driven and self-motivated.
  • Strong interpersonal and communication skills (verbal and presentation).
  • Organized, with strong computer literacy such as MS Project, Excel, etc.

Other Requirements

Location: Indianapolis

Travel: Up to 25% of the time to various suppliers, collaborators, and client sites

Compensation

Competitive Salary and Benefits Package

Job Type: Full-time

Benefits:

  • 401(k)
  • 401(k) matching
  • Dental insurance
  • Health insurance
  • Health savings account
  • Life insurance
  • Paid time off
  • Referral program
  • Vision insurance

Experience level:

  • 5 years

Schedule:

  • 8 hour shift
  • Monday to Friday

Ability to commute/relocate:

  • Indianapolis, IN 46218: Reliably commute or planning to relocate before starting work (Required)

Willingness to travel:

  • 25% (Required)

Work Location: One location




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