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Open nowFirst seen 44 hours ago

DeltaV Engineer

KLM145 open roles

Where
Kalamazoo, Michigan, United States
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Your applicationOpen nowDeltaV EngineerKLM · Kalamazoo, Michigan, United States

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Share of postings closed within
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  2. 4.4%3 days
  3. 11.8%7 days
  4. 18.6%14 days
  5. 35.6%30 days
  6. 45.1%60 days
This job: first seen 44 hours ago

The posting

DeltaV Engineer

Kalamazoo, MI

Must be a US Citizen or Green Card holder.

  • We have a DeltaV Engineer opportunity in Kalamazoo, MI. As a DeltaV Engineer, you will play a critical role in designing and implementing advanced Emerson DeltaV automation solutions for the Life Sciences industry.
  • Working within a dynamic system integration environment, you will be part of a team responsible for delivering high-quality, fit-for-purpose, regulatory-compliant automation that supports biopharmaceutical and medical device manufacturing.
  • This is an opportunity to contribute to projects that impact global healthcare while growing within an employee-owned organization that values innovation and technical excellence.
  • You will have the opportunity to work in one of our local offices while supporting clients nationwide, delivering cutting-edge automation solutions in the industry.

RESPONSIBILITIES:

  • All areas of responsibility listed below are essential to the satisfactory performance of this position, with reasonable accommodation, if necessary.
  • Develop, configure, and implement Emerson DeltaV control systems, ensuring alignment with customer specifications, Wunderlich-Malec (WM) standards, and industry best practices
  • Design and program DeltaV batch processes per ISA-88 standards
  • Collaborate with clients in the life sciences industry to gather requirements and develop customized automation solutions
  • Engineer system architecture, instrument specifications, and control strategies to optimize manufacturing efficiency
  • Configure DeltaV controllers, applications, HMI, and historian solutions while ensuring compliance with GAMP 5, cGMP, and 21 CFR Part 11 regulations
  • Conduct Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT) to validate system performance
  • Provide on-site startup, commissioning, and troubleshooting support activities for deployed systems into production environments
  • Ensure compliance with system and software development life cycle methodologies, including validation documentation
  • Work closely with multidisciplinary teams, including electrical engineers, process engineers, validation engineers, and project managers, to deliver projects on time and within budget
  • Mentor junior engineers and technicians, fostering knowledge-sharing and technical growth

QUALIFICATIONS:

  • Professional degree in Electrical Engineering, Control Systems Engineering, Chemical Engineering, or a related field
  • 3 to 7 years of experience in automation and control system engineering, preferably with a focus on Emerson DeltaV
  • Proficiency in ISA-88 Batch Processing and DeltaV Batch configuration
  • Familiarity with Historian, Alarm Management, and Advanced Control Strategies
  • Experience with automation protocols (HART, Foundation Fieldbus, Profibus, Modbus TCP/IP, Ethernet/IP, OPC)
  • Expertise in process control strategies, loop tuning, and system integration
  • Understanding of industrial networking for communication between controllers, servers, and HMIs
  • Working experience in the Life Sciences industry, including biotechnology, pharmaceuticals, or medical devices is preferred, but not required if strong Emerson DeltaV experience from other industries
  • Knowledge of GAMP5, cGMP, 21 CFR Part 11, and validation life cycle processes
  • Familiarity with electrical design principles and working knowledge of AutoCAD is a plus
  • Strong troubleshooting skills and the ability to diagnose and resolve complex automation issues
  • Familiarity with Rockwell Automation, Siemens PCS7, or other DCS/SCADA systems is a plus
  • Willingness to travel up to 25% for on-site support and commissioning
  • Ability to work independently and collaboratively on complex automation projects in industrial and manufacturing environments
  • Strong written and verbal communication skills for technical documentation and collaboration with cross-functional teams and clients.
  • Passion for craftmanship, innovation, and problem-solving in mission-critical environments.
  • Professional references from a peer and a manager
  • Experience in translating high-level functional requirements into detailed software design

Working Conditions:

  • The work environment characteristics described here represent those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform essential functions.
  • Office Work:
  • Office desk/cubicle environment
  • Frequent use of computers, engineering tools, and industrial control systems
  • Physical Demands:
  • Occasional lifting, climbing, and working in production facilities during commissioning activities
  • Work may include working weekends, holidays, nightshift, and extended hours to meet deadlines and client requirements.

Our People:

  • Empowered Individuals Employee-owned, we are able to hire the best and empower them to develop and deliver solutions
  • Rewarded & Motivated Investing in continuing education and world-class benefits keeps our staff motivated
  • Positive Attitudes Dedicated experts are committed in the long run and bring a positive, can-do attitude to your project
  • Knowledgeable Recognized industry experts reinforced with ongoing training remain knowledgeable on the latest industry trends and directions

Required Knowledge, Skills, and Abilities: (Companies ATS Questions):

1. Life Science/Pharma industry experience

2. Extensive hands-on experience with Emerson DeltaV systems (design, implementation, configuration) AND PLC

3. Experience with ISA-88 Batch Processing and DeltaV Batch configuration

4. Familiarity with automation protocols such as Ethernet/IP, Modbus TCP/IP, Profibus, OPC, Foundation Fieldbus, and HART

5. Experience working in or supporting Life Sciences, Biotech, Pharmaceutical, or Medical Device environments

6. Strong knowledge of GAMP5, cGMP, and 21 CFR Part 11

7. Experience conducting FAT/SAT, startup, and commissioning

8. Ability to troubleshoot and resolve complex automation issues

9. Strong communication skills for cross-functional collaboration

10. Ability to work independently or as part of a team on industrial/manufacturing automation projects

11. Willingness to travel up to 25% and work extended hours or weekends if needed

12. Knowledge of historian systems, alarm management, and advanced control strategies - Nice to have:

13. Familiarity with industrial networking (controllers, HMIs, servers) - Nice to have:

14. Exposure to Rockwell Automation, Siemens PCS7, or other DCS/SCADA platforms - Nice to have:

15. Working knowledge of AutoCAD and electrical design principles - Nice to have:

16. Experience with loop tuning and process control optimization - Nice to hav

17. Experience mentoring junior engineers or technicians - Nice to have:

18. Experience translating functional specs into detailed software design - Nice to have:

19. Previous experience working on mission-critical or regulated environments - Nice to have:

20. Professional references from a peer and a manager- Nice to have:

21. Must be a US Citizen or Green Card holder.

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