Senior Controls Engineer - Automation
Required skills
- Pharmaceutical
- GMP
- automation
- controls
- validation
- DCS/PLC integration
- logistics automation
- commissioning
- qualification
- Allen-Bradley
Nice to have
- Emerson DeltaV
- travel
Role summary
ACE Technologies is seeking a Senior Pharmaceutical Controls Engineer in Indianapolis, IN. This full-time, onsite role involves designing, developing, and supporting automation and control systems within GMP-regulated pharmaceutical manufacturing facilities. Responsibilities include programming Emerson DeltaV and Rockwell PLC platforms, supporting commissioning and validation, and collaborating with quality and operations teams. The ideal candidate has 8+ years of relevant experience, hands-on controls and automation experience in operating pharma facilities, and familiarity with structured compliance and documentation practices. Experience with SCADA systems like FactoryTalk or Ignition is required.
Senior Pharmaceutical Controls Engineer
Location: Indianapolis, IN (Primarily Onsite)
Company: ACE Technologies, LLC
Employment Type: Full-Time
About ACE Technologies
ACE Technologies is a system integrator specializing in automation, controls, and validation within Life Sciences and pharmaceutical manufacturing environments. Our team supports DCS/PLC integration, logistics automation, commissioning & qualification, and complex system implementations inside GMP-regulated facilities. We operate primarily in Indianapolis and throughout the eastern United States, partnering directly with pharmaceutical manufacturers to deliver high-quality automation solutions.
Position Overview
We are seeking a Senior Pharmaceutical Controls Engineer to join our growing team in Indianapolis. This is a project-based, client-facing role working onsite within pharmaceutical manufacturing facilities. Travel may occasionally be required (e.g., Raleigh, NC), but the role is primarily local to Indianapolis.
The engineer will work alongside a strong internal technical team while interfacing directly with client stakeholders in structured, GMP-regulated environments.
Key Responsibilities
- Design, develop, and support control systems within pharmaceutical manufacturing facilities
- Program and configure Emerson DeltaV and/or Rockwell PLC platforms
- Support commissioning, qualification, and validation activities
- Collaborate with validation, quality, and operations teams
- Review technical design documentation and test strategies
- Support automated systems including ASRS, conveyors, logistics platforms, and integrated systems
- Function independently as a technical SME when required
- Maintain compliance within structured GMP documentation environments
Required Qualifications
- Direct experience in pharmaceutical / GMP-regulated manufacturing environments
- Hands-on controls and automation experience inside operating pharma facilities
- Experience working alongside validation / quality teams
- Strong familiarity with structured compliance and documentation practices
- Allen-Bradley / Rockwell PLC experience (required)
- Emerson DeltaV experience (strongly preferred)
- SCADA experience (FactoryTalk, Ignition, etc.)
- Approximately 8+ years of relevant experience
- Ability to work onsite in Indianapolis pharmaceutical facilities
What We Are NOT Looking For
- General manufacturing automation backgrounds without GMP exposure
- Panel-only PLC programmers without pharmaceutical experience
- Candidates requiring extensive training
- Individuals who have only managed integrators without performing hands-on controls work
Work Authorization
ACE Technologies is focused on candidates who are already authorized to work in the United States without the need for current or future visa sponsorship. Green Card holders are welcome to apply.
Why Join ACE?
- Primarily local role with limited travel
- Exposure to complex pharmaceutical automation environments
- Strong internal technical team support
- Client-facing, high-impact project work
- Growth opportunity within Life Sciences automation
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