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LVI Associates

DeltaV Engineer

LVI Associates, Boston, Massachusetts, United States, 02298

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Position:

DeltaV Automation Engineer Location:

Greater Boston Area Experience Levels: Mid-Level: 3-7 years Senior: 7-14 years Principal: 14+ years

Overview

A leading engineering and consulting firm in the life sciences sector is seeking experienced

DeltaV Automation Engineers

to support projects in the

biotech and pharmaceutical industries . With over two decades of global experience, the firm specializes in manufacturing applications including process automation, MES, data analytics, and project management. This is an excellent opportunity to join a dynamic team working on the design, automation, commissioning, and startup of cutting-edge facilities and systems. The ideal candidate will bring strong technical expertise, hands-on automation skills, and solid documentation capabilities.

Key Responsibilities

Design, configure, and implement process control solutions for life sciences manufacturing Program, test, and document

Emerson DeltaV DCS

systems Develop user requirements, software/hardware design specifications, and validation protocols Create electrical panel schematics and scope of supply documentation Lead and manage automation projects, ensuring timely progress and delivery Support on-site installation, testing, and startup of control systems Collaborate with plant engineers and operators to optimize control strategies Provide training to operators and engineering staff on control systems

Qualifications

Bachelor's or Master's degree in Mechanical, Chemical, or related Engineering discipline Proven experience in the

biotech/pharma industry Strong understanding of

S88 Batch structure

and

DeltaV architecture Proficient in reading and interpreting

P&IDs

and automation narratives Hands-on experience with commissioning and startup of control systems Familiarity with

PLC, HMI, and SCADA

platforms (Rockwell, Siemens, Wonderware, GE) Knowledge of control system networking (TCP/IP, Ethernet/IP, OPC UA, Profibus) Understanding of

cGMP ,

FDA regulations , and

21 CFR Part 11

compliance