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HVAC Engineer – Siemens & BMS Support

Automated Systems

Kenosha, Wisconsin

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JOB DETAILS
SKILLS
Automation, Automation Engineering, Biotech and Pharmaceutical, Change Control, Consulting, Distributed Control Systems (DCS), Document Control, Documentation, Drug Manufacturing, Engineering, Establish Priorities, Facilities Engineering, GMP (Good Manufacturing Practices), HVAC, Identify Issues, Illustrating Ability, Quality Metrics, Site Acquisition, System Integration (SI), Technical Writing
LOCATION
Kenosha, Wisconsin
POSTED
25 days ago

HVAC Engineer – Siemens & BMS Support

Contract: 12-18 months duration

Location: Kenosha County, WI – Onsite On-site, Kenosha County, WI.

Work: Standard business hours with occasional coordination needs outside core hours.


Role Summary

ASI is seeking an experienced HVAC Engineer to support HVAC troubleshooting, Siemens and BMS activities at the Kenosha County site, a recently acquired facility transitioning from legacy pharmaceutical systems. 


Key Responsibilities

•     Perform gap assessment of existing BAS/DCS drawings against Quality Standards (QS) and Global Quality Standards (GQS)

•     Execute redline markups and formal drawing revisions for automation-related P&IDs, loop diagrams, and instrument indexes

•     Collaborate with Automation and Facilities engineering leads to prioritize remediation sequence aligned with Phase 2 system acceptance milestones

•     Support BAS/DCS alignment activities including configuration review, alarm rationalization, and documentation updates

•     Coordinate with the Engineering Technical Writer to route revised documents through GMP document control (Veeva/MasterControl)

•     Participate in QBMS alarm coverage handoff planning as the long-term automated solution is developed

•     Contribute to change control packages (MOCs) as required for documented system changes



Requirements

Required Qualifications

•     3–7+ years of automation engineering experience in a GMP pharmaceutical or biotech manufacturing environment

•     Hands-on experience with BAS/DCS platforms — Rockwell, Siemens Desigo CC, or equivalent

•     Proficiency in reading and revising engineering drawings: loop sheets, P&IDs, instrument indexes, wiring diagrams

•     Familiarity with GMP documentation requirements and change control procedures

•     Experience with drawing remediation, document lifecycle management, or legacy system integration projects


Preferred Qualifications

•     Familiarity with Quality Standards (QS) or equivalent large-pharma quality frameworks

•     Experience with Veeva QualityDocs or MasterControl for GMP document routing

•     Exposure to site acquisition / system integration projects

•     CSIA certification or equivalent automation professional credential

 



About the Company

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Automated Systems