drjobs Senior Automation Engineer Controls

Senior Automation Engineer Controls

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1 Vacancy
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Job Location drjobs

Wilmington, NC - USA

Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Overview: We are seeking a Senior Automation Engineer with strong expertise in PLC DCS HMI and SCADA platforms. This role involves leading a team of engineers working directly with clients to identify requirements and delivering innovative automation solutions.

Key Responsibilities:

  • Develop and implement control systems for industrial processes and machinery.
  • Design system architecture select components create schematics and program controllers.
  • Implement and commission control systems onsite.
  • Lead project management tasks including budgeting scheduling and team coordination.
  • Ensure project profitability and customer satisfaction.

Qualifications:

  • Bachelor s degree in Electrical/Control Engineering Mechanical Engineering Chemical Engineering or Computer Science.
  • 10 years of experience in automation engineering.
  • Proficiency in PLC HMI/SCADA and DCS platforms (e.g. Rockwell Automation Siemens Emerson DeltaV).
  • Familiarity with industrial networking protocols and electrical schematics.
  • Experience leading engineering teams and managing projects in the Life Science industry.
  • Knowledge of regulatory requirements such as cGMP and 21 CFR Part 11.
  • Strong communication skills and technical writing ability.
  • Willingness to travel up to 25%.

Benefits:

  • Competitive salary and benefits package.
  • Opportunity to work with a growing company in a leadership role.


Bachelor s degree in Electrical/Control Engineering, Mechanical Engineering, Chemical Engineering, or Computer Science. 10+ years of experience in automation engineering. Proficiency in PLC, HMI/SCADA, and DCS platforms (e.g., Rockwell Automation, Siemens, Emerson DeltaV). Familiarity with industrial networking protocols and electrical schematics. Experience leading engineering teams and managing projects in the Life Science industry. Knowledge of regulatory requirements such as cGMP and 21 CFR Part 11. Strong communication skills and technical writing ability. Willingness to travel up to 25%.

Employment Type

Full Time

Company Industry

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