Automation Lead – PLC / DeltaV (USA)

  • Indianapolis, Indiana, United States
  • Engineering
  • Full-Time
  • On-Site

Job Description:

Advanced Manufacturing Tech Solutions (AMTSOL) - www.amtsol.com

A leader in Life Science Manufacturing Technology solutions, we are looking for top talent to be part of the dynamic team and drive the growth of the business.

Title: Automation Area Lead – DeltaV

  • Location: Indiana, IN (Hybrid)
  • Minimum 1 week a month in Indiana during the basic/detailed design phase of the project. Full time on site during the Commissioning phase of the project
  • Project based role, Duration 3 years
  • Budget is open

The Program Technical Office (PTO) defines and governs the overall automation philosophy, standards, and technical consistency across all facilities within the program.

The PTO Automation Lead – PLC/DeltaV will provide technical ownership and governance for PLC-based equipment (e.g., Lyophilizers and hybrid process systems), ensuring alignment with the programs automation strategy, S88 standards, DeltaV architecture, and GMP/CSV requirements.

This role acts as the technical bridge between OEM PLC systems, System Integrators, and the PTO governance framework.

Key Responsibilities

  • Provide technical ownership for PLC-based systems within assigned manufacturing areas.
  • Reverse engineer OEM PLC control strategies and align/integrate them into the DeltaV Batch DCS architecture.
  • Define and govern S88 software structure, phases, recipes, and control strategies.
  • Develop and review Functional Design Specifications (FDS) and automation requirements.
  • Ensure automation deliverables align with overall PTO standards and automation philosophy.
  • Collaborate with Automation Project Managers, Technical Leads, Process Engineers, Quality, and Operations.
  • Oversee and guide System Integrators on detailed design, coding, and testing activities.
  • Support P&ID reviews, control strategy reviews, and system architecture alignment.
  • Ensure compliance with GMP, regulatory standards, and CSV principles.
  • Review validation deliverables including alarm rationalization, system overview, and testing documentation.
  • Support issue tracking, risk identification, and remediation planning.
  • Provide technical consulting and guidance within the PTO governance structure.

Requirements

  • Bachelors Degree in Engineering (or equivalent experience).
  • 8–10+ years of automation experience in pharmaceutical or biotech manufacturing.
  • Strong experience in Allen-Bradley PLC systems (5+ years).
  • Hands-on experience with DeltaV Batch DCS (3+ years preferred).
  • Experience with Lyophilizers or hybrid drug substance manufacturing systems preferred.
  • Proven experience in large-scale GMP automation programs.
  • Strong understanding of ISA-88, GMP, regulatory requirements, and Computer System Validation (CSV).
  • Ability to work within a structured program governance model (PTO).
  • Strong stakeholder management and cross-functional collaboration skills.