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.