Automation Project Manager
Hybrid · Indianapolis, Indiana, United States
Job Summary
Automation Project Manager responsible for delivering the automation solution for GMP clinical trial drug substance facilities on a greenfield site. Lead and coordinate Automation Project Teams, define hardware/software requirements, standards, and oversee system integrators. Collaborate with MES, BMS, and Data Historian project managers, prepare proposals and bid analyses, drive risk assessment, change control, schedule and cost management, and report progress to the PMO. Requires leadership across multiple facilities, hands-on experience in DeltaV-controlled projects, strong project-management skills, and deep knowledge of GMP/regulatory validation. Hybrid work arrangement with Indiana-based on-site needs during commissioning.
Required Qualifications
- BS in Engineering or equivalent experience
- 10+ years of automation experience in the pharmaceutical industry
- Experience delivering large automation projects in the pharmaceutical industry
- 5+ years of experience in DeltaV controlled/batch-based capital projects
- Proficiency with project management tools (e.g., P6/MS Project)
- Excellent written and verbal communication skills for technical and non-technical audiences
- Strong knowledge of GMPs, regulatory requirements, and computer system validation
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