DeltaV Automation Engineer

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

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