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(Job RF -1119) DeltaV Engineer

Ash & Harris Executive Search is looking for a DeltaV Automation Engineer

Overview:
Join an employee-owned engineering leader as a DeltaV Engineer, playing a critical role in designing and implementing advanced automation solutions for the Life Sciences industry. You will deliver high-quality, regulatory-compliant systems for biopharmaceutical and medical device manufacturing clients nationwide. This position is based in Kalamazoo, MI, and offers the opportunity to work on impactful projects within a culture that values innovation and technical excellence.

Key Responsibilities:

  • Design, develop, configure, and implement Emerson DeltaV control systems.
  • Program and design DeltaV batch processes in accordance with ISA-88 standards.
  • Collaborate with clients to gather requirements and develop customized automation solutions.
  • Engineer system architecture, instrument specifications, and control strategies.
  • Configure DeltaV controllers, HMI, and historian solutions, ensuring compliance with GAMP 5, cGMP, and 21 CFR Part 11.
  • Conduct and support Factory (FAT) and Site Acceptance Testing (SAT).
  • Provide on-site startup, commissioning, and troubleshooting support.
  • Ensure compliance with system development life cycle and validation documentation requirements.
  • Work with cross-functional teams (electrical, process, validation engineers, project managers) to deliver projects on time and within budget.
  • Mentor junior engineers and technicians.

Requirements:

Education

  • Bachelor’s degree in Electrical Engineering, Control Systems Engineering, Chemical Engineering, or a related field.

Experiences

  • 3 to 7 years of automation and control system engineering experience.
  • Proven, hands-on experience with Emerson DeltaV systems is essential.
  • Proficiency in DeltaV Batch configuration and ISA-88 standards.
  • Experience with industrial automation protocols (e.g., HART, Foundation Fieldbus, Profibus, Modbus TCP/IP).
  • Working experience in the Life Sciences industry (biotech, pharma, medical devices) is highly preferred.
  • Knowledge of GAMP5, cGMP, 21 CFR Part 11, and validation processes.
  • Experience with system commissioning, FAT, and SAT.

Other

  • Willingness to travel up to 25% for on-site client support.
  • Strong troubleshooting and problem-solving skills.
  • Excellent written and verbal communication skills.
  • Ability to work independently and collaboratively in a team environment.
  • Must provide professional references from a peer and a manager.

Compensation and Benefits:

Salary

  • A competitive salary commensurate with experience will be offered.

Benefits

  • Comprehensive benefits package.
  • Investment in continuing education.
  • Participation in a 100% Employee-Owned (ESOP) company.

Schedule:

Full-time

  • Permanent, full-time position.

Work arrangement:

  • On-site (Kalamazoo, MI office). Role includes travel to client sites up to 25% of the time.

Average salary estimate

$107500 / YEARLY (est.)
min
max
$90000K
$125000K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

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EMPLOYMENT TYPE
Full-time, onsite
DATE POSTED
August 22, 2025
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