DeltaV Automation Engineer – Life Sciences

JC Automation Corp.

Maryland

Hybrid

USD 85,000 - 110,000

Full time

7 days ago
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Job summary

JC Automation Corp. is seeking an Intermediate Automation Engineer with Emerson DeltaV experience to support a life sciences site in Walkersville, Maryland.

The role involves configuring, troubleshooting, testing, commissioning, and continuous improvement of automation systems in a regulated manufacturing environment. The ideal candidate has a bachelor’s degree in engineering and at least 3 years of relevant experience, with hands-on DeltaV expertise and GMP documentation practices, and must be

Qualifications

  • Bachelor's degree in Engineering or related technical field.
  • Approximately 3+ years of automation/controls experience.
  • Hands-on Emerson DeltaV experience.
  • Experience in regulated manufacturing environments (pharma, biotech, life sciences).

Responsibilities

  • Configure, maintain, troubleshoot, and optimize Emerson DeltaV control systems.
  • Support automation activities for manufacturing equipment and process systems.
  • Assist with commissioning, startup, FAT/SAT, loop checks, and testing.
  • Develop and maintain automation documentation (configurations, narratives, test records).
  • Collaborate with engineering, maintenance, operations, quality, and validation teams.

Skills

DeltaV knowledge
Troubleshooting
Communication
Teamwork
On-site work

Education

Bachelor's degree in Engineering, Automation, Controls, Electrical, Computer Engineering or related field

Tools

Emerson DeltaV

Job description

JC Automation Corp. is seeking an Intermediate Automation Engineer with Emerson DeltaV experience to support a life sciences site in Walkersville, Maryland.

The role involves configuring, troubleshooting, testing, commissioning, and continuous improvement of automation systems in a regulated manufacturing environment. The ideal candidate has a bachelor’s degree in engineering and at least 3 years of relevant experience, with hands-on DeltaV expertise and GMP documentation practices, and must be

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