Senior Automation Engineering

PACIV4 months ago
Indianapolis, IN, United States
On-site
Full-time
Junior Level (1-3 years)

Job Description

Senior DeltaV Automation Engineer - Emerson DeltaV Batch Experience Required

We are a global leader in industrial automation and process control solutions, serving clients in the life sciences, pharmaceutical, medical device, food & beverage, and utilities sectors, specializing in delivering compliant, high-performance automation systems tailored to regulated environments.

We are looking for a Senior DeltaV Automation Engineer for our Indianapolis, IN office who can drive impactful automation solutions across biotechnology and life sciences sectors. This role combines strategic technical leadership with hands‑on implementation of industrial control systems. Support proposal development, lead automation projects, and provide day‑to‑day troubleshooting and maintenance for platforms for Emerson DeltaV Batch, Allen‑Bradley PLCs, and iFix within pharmaceutical manufacturing environments.

Design, develop, and install Emerson DeltaV based automation systems for manufacturing and skid package integration. Apply ISA-88 batch control principles to design and configure modular, scalable batch automation solutions using FactoryTalk Batch and DeltaV platforms, ensuring consistency and flexibility in life sciences manufacturing processes.

Support and maintain DeltaV Distributed Control Systems to ensure reliable automation of life sciences manufacturing processes, including batch control, equipment integration, and system optimization.

Develop and maintain SCADA HMI interfaces to enable efficient monitoring and control of manufacturing operations.

Contribute to capital projects by supporting system design, installation, commissioning, testing, and modernization of automation infrastructure.

Lead initiatives for remediation, migration, and upgrades of legacy automation systems to enhance reliability, compliance, and performance.

Collaborate with the Validation Team to ensure automation systems align with regulatory and quality standards by applying expertise in cGMP, GAMP, and 21 CFR Part 11 throughout design, implementation, and validation activities.

Leverage OSI PI or equivalent Data Historian systems to monitor, archive, and analyze process data, supporting continuous improvement and regulatory compliance in life science manufacturing environments.

We do not consider C2C (Corp-to-Corp) or 1099 contract arrangements.

Qualifications

  • Bachelor’s or Master’s degree: in Electrical or Chemical Engineering
  • Proven ability in control system design, programming, troubleshooting, and implementation within regulated environments.
  • Hands‑on experience with system integration and process control systems for Allen‑Bradley SLCs, ControlLogix, iFIX, Foundation Fieldbus, and DeviceNet
  • Working knowledge of Data Historian systems, particularly OSI PI.
  • Understanding of Computer System Validation lifecycle and FDA regulatory requirements.

Equal Employment Opportunity

All qualified candidates will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other legally protected status.

PACIV complies with all applicable federal, state, and local laws regarding non‑discrimination and affirmative action.

Benefits

  • Medical insurance
  • Disability insurance

Required Skills

FDA Regulatory Compliance
Data Historian Systems (OSI PI)
cGMP
FactoryTalk Batch
Automation System Design
Process Control
GAMP
iFix
Batch Control Systems
Allen-Bradley PLCs
Emerson DeltaV
System Integration
SCADA HMI Interfaces