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LVI Associates

DeltaV Automation Engineer

LVI Associates, Boston, Massachusetts, us, 02298

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Base pay range

$100,000.00/yr - $140,000.00/yr Job Title

DeltaV Automation Engineer (Biotech/Pharmaceutical) Overview

An experienced DeltaV Automation Engineer is sought to support engineering and consulting projects within the biotechnology and pharmaceutical industries. The role involves working with a team of engineers on the design, automation, commissioning, and start-up of various processes, systems, and facilities. This is an excellent opportunity to join a growing team in the life sciences sector and expand professional development. Areas of Expertise

Process and Facility Automation Project Management Manufacturing Execution Systems (MES) Data Analytics Responsibilities

Design, configure, integrate, and implement process control solutions for life sciences applications. Program, implement, test, and document Emerson DeltaV Distributed Control Systems (DCS). Develop User Requirement Specifications and Software/Hardware Design Specifications. Create control system validation and testing protocols. Design electrical panel schematics and scope of supply documents. Manage assigned automation projects and monitor progress. Install, test, and start up control systems on-site. Collaborate with plant engineers and operators to implement control strategies. Train operators and engineers on control systems. Qualifications

Bachelor's or Master's degree in Mechanical Engineering, Chemical Engineering, or a related discipline. Minimum of 5 years of experience in the biotech/pharma industry. Strong knowledge of the ISA-88 Batch structure. Proficiency in reading and interpreting P&ID drawings. Deep understanding of automation narratives and DeltaV architecture. Experience in commissioning and startup of control systems. Familiarity with PLC, HMI, and SCADA systems is a plus. Knowledge of control system networking and PC networking technologies. Experience with SCADA platforms such as Rockwell, Siemens, Wonderware, and GE is advantageous. Specific knowledge of cGMPs and batch process control in the life sciences industry. Understanding of regulatory compliance including cGMP, 21 CFR Part 11, and FDA regulations. Seniority Level

Mid-Senior level Employment Type

Full-time Industries

Pharmaceutical Manufacturing Benefits

Medical insurance Vision insurance 401(k) Tuition assistance Note

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