LVI Associates
Base pay range
$120,000.00/yr - $150,000.00/yr
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
Seniority level
Mid‑Senior level
Employment type
Full‑time
Job function
Pharmaceutical Manufacturing
Location Cambridge, MA
Benefits
Medical insurance
Vision insurance
401(k)
Tuition assistance
#J-18808-Ljbffr
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
Seniority level
Mid‑Senior level
Employment type
Full‑time
Job function
Pharmaceutical Manufacturing
Location Cambridge, MA
Benefits
Medical insurance
Vision insurance
401(k)
Tuition assistance
#J-18808-Ljbffr